Anthracyclidine-acetic acid derivatives



United States Patent US. Cl. 260351 12 Claims ABSTRACT OF THE DISCLOSURE The total synthesis of tetracycline-type antibiotics by a multi-step process beginning with 3,4,l0-trioXo-1,2,3,4, 4a,9,9a,lO-octahydroanthracenes comprising: (1) an aldol condensation with a glyoxalic acid ester to give a 2-carboxymethylidene 3,4,10 trioxo-1,2,3,4,4a,9,9a,l0-octahydroanthracene ester; (2) Michael reaction of said ester with an amine to produce a 3,4,10-trioxo-1,2,3,4,4a,9,9a, 10-octahydroanthracene-Z-(oz-amino) acetic acid ester; (3) conversion of the triketone to the corresponding 4,10- diketone by (a) selective reduction of the Michael reaction product to the corresponding 3-hydroxy compound, followed by conversion of the 3-hydroxy compound to the corresponding 3-formyloxy compound and removal of the 3-formyloxy group by treatment with zinc dust to give a 4,l0-dioxo-1,2,3,4,4a,9,9a,10-octahydroanthracene 2-(tx-amino)acetic acid ester; or (b) conversion of the hydrochloride salt of the Michael reaction product to a lactone by reaction with p-toluene'sulfonic acid and treatment of the lactone with zinc dust formic acid; (4) conversion of the 4,10-diketo-1,2,3,4,4a,9,9a,10-octahydroanthracene 2-(a-amino)acetic acid to a mixed anhydride; (5) followed by acylation of a malonic acid ester with the mixed anhydride; (6) cyclization of the acyl malonate derivative to a l2a-deoxytetracycline which is then hydroxylated to a tetracycline. The preparation of the 3,4,10-trioxo-1,2,3,4,4a,9,9a,10 octahydroanthracenes from benzoyl halides by (a) Friedel-Crafts reaction of a benzoyl halide with a pyrocatechol ether, e.g., a di-(lower)alkyl ether, to produce a 3,4-di(lower)alkoxybenzophenone; (b) conversion of the benzophenone by partial or complete reduction of the carbonyl group by chemical or catalytic methods to a 3,4-di(lower)alkoxy diphenyl methanol or 3,4-di-(lower)alkoxy diphenyl methane; or to a 3,4-di-(lower)alkoxy diphenyl alkane via a Grignard reaction and reduction of the thus-produced alkanol; (c) oxidation of the 3,4-di-(lower)alkoxy diphenyl alkane, or the corresponding dihydroxy compound, to a dienedioic acid ester or dienedioic acid; ((1) hydrogenation of the di enedioic acid compound to a benzyl adipic acid derivative; (e) cyclization of said compound to a 2-(2-carbalkoxyethyl)-4-tetralone by means of dehydrating or dehydrohalogenating agents; (f) cyelization of the 4-tetralone derivatives by condensation with a dialkyloxalate to give a Z-carbalkoxy 3,4,l0-trioxo-octahydroanthracene; and (g) removal of the 2-substituent by decarboxylation. The intermediates and final products are useful as bactericides and/ or chelating agents.

This application is a continuation-in-part of our earlier filed pending application Ser. No. 209,269, filed July 11, 1962, which, in turn, is a continuation-in-part of application Ser. No. 132,304, filed Aug. 18, 1961, and now abandoned.

This invention relates to a process of preparation of antibacterial agents. More particularly, it is concerned with the discovery of new and novel synthetic routes for the preparation of known as well as new tetracycline products. It is also concerned with the new and useful tetracycline products obtained thereby, as well as with the new intermediates of the process.

The tetracycline antibiotics comprise a group of biologically active hydronaphthacene derivatives having the following essential structural features. The numbering system indicated is that employed by Chemical Abstracts.

Among the biologically active members of this group are those containing the following substituent groups:

Substituents Common Name 4-N(OH )2, 6-OH, 6-CH3, 12a-OH.-. Tetracycline.

5-OH, 6-CH 12a-0H, fi-OH 4-desdimethylaminoo-oxytetracyc me. 4-N(CH )Q, 6'CH3, 12a-OH fi-deoxytetracyeline.

fi-deoxy-G-demethyltetracycline. 7-bromotetracyeline.

6-demethyl-7-chlorotetracycline.

60H, 6-CI-I ,12a- H 4-desdimethylaminotetracycline.

6-OH, G-OH 7-01, l2a-OH 4-desdimethylamino-7-ehlorotetracycline.

4-N(CH3)2, G-OH, l2a-OH. G-demethyltetracycllne.

12a-OH 6-de0xy-G-demethyl-4-desdimethylaminotetracycline.

The present new processes utilize 3,4,10-trioxo-1,2,3,4, 4a,9,9a,lO-octahydroanthracenes, Formula I, as starting materials to produce both known and new tetracyclines having the formulae wherein the various terms are as defined below, by the reaction sequence illustrated in Flow Sheet I. It will be appreciated by those skilled in the art that several alternative routes exist for the conversion of compounds of Formula I to the final products of Formulae XVI and XVII. The particular route adopted for the preparation of a given tetracycline is largely dependent upon economic factors, such as availability of materials, and yields of reaction products throughout the sequence.

Further, the conditions for any reaction in the sequence can, unless otherwise indicated, be varied within the skill of the art. The actual conditions employed are determined by the above listed factors as well as by type and availability of equipment.

In the compounds of this sequence, X is selected from the group consisting of hydrogen, hydroxy, triiluoromethyl, amino, mono and di-lower alkylamino, alkanoylamino containing 2 to 4 carbon atoms, lower alkyl, alkanoyloxy containing 2 to 4 carbon atoms; and OR wherein R is selected from the group consisting of lower alkyl and benzyl;

X is selected from the group consisting of hydrogen, chloro, lower alkyl and trifiuoromethyl;

X is selected from the group consisting of hydrogen, hydroxy, and OR in which R is as previously defined;

A is selected from the group consisting of hydrogen, lower alkyl, and B OCH(B wherein B is lower alkyl and B is selected from the group consisting of hydrogen and lower alkyl;

X is selected from the group consisting of hydrogen, lower alkyl and benzyl;

R is selected from the group consisting of X and CO X (mixed anhydride) in which X is lower alkyl;

R and B, when taken together with the nitrogen atom to which they are attached form a nitrogen heterocyclic ring selected from the g roup consisting of piperazyl, piperidyl, morpholinyl, pyrryl, pyrrolidyl, Z-(lower carbalkoxy)pyrr olidyl, and thiomorpholinyl; 7

R and R when taken separately are each selected from the group consisting of hydrogen, alkanoyl containing 1 to 4 carbon atoms, and CH B wherein B is selected from the group consisting of hydrogen, lower alkyl, and monosubstituted lower alkyl, said substituent being selected from the group consisting of hydroxy and lower alkoxy;

Provided that only one of said R and R substituents is selected from the group consisting of alkanoyl containing l to 4 carbon atoms;

X is selected from the group consisting of cyano and i C-NHRs wherein R is selected from the group consisting of hydrogen and lower alkyl; X is selected from the group consisting of CH CHOH,

if -CH(O CH) and C O;

Y is selected from the group consisting of cyano and lower carbalkoxy.

It should be noted that although the X, X and X terms in the benzenoid moiety of the above generic structures appear in the same sequence, they need not be present in this sequence in actual practice. This representation is for convenience only and is not to be taken to indicate, for example, that X; always represents the S-Substituent, or that X represents the 6- or the 7-substituent. They can occur in any sequence in the benzenoid moiety.

It should be noted that the various substituents in the final tetracyclines of Formulae XVI and XVII or in the intermediates for their production may be replaced by other groups according to procedures described hereinafter. Thus, X, X and X may be transformed to hydroxy, hydroxyalkyl, nitro, cyano, carbalkoxy, alkyl sulfonyl, halo sulfonyl alkyl sulfinyl, and sulfarnyl. The A substituent may be transformed to CHB amino, monoor di-lower alkylamino and CH(B )OH wherein B is selected from the group consisting of hydrogen and alkyl, by appropriate reactions as is disclosed below.

A wide variety of 4-aminotetracyclines are, of course, prepared according to the present processes by substituting various primary or secondary alkyl, aralkyl, or aryl amines for dimethylamine. Suitable amines include other dialkylamines, e.g. methyl, ethyl, propyl, etc. amines; aralkyl and alkaryl amines, and N-alkyl derivatives thereof, eg, N-methylaniline, benzylamine, heterocyclic amines, e.g. pyrrolidine, morpholine, aminopyridines and N-alkyl derivatives thereof; arylamines, e.g. aniline and substituted derivatives thereof wherein the substituent is hydroxy, carbalkoxy, nitro and amino; and ammonia. Further, hydroxyalkyl substituents on the nitrogen where protected for some of the reaction steps by ether formation or acylation, as discussed below, may subsequently be regenerated, e.g., by HBr cleavage or hydrolysis.

Of the present new compounds of particular value are those containing the following benzenoid moiety:

in which X, X and OR are as described above since these compounds are suitable for the preparation of known and biologically active tetracycline compounds, i.e. Where OR is OH and, in addition, new and useful tetracycline compounds not previously described.

From I to XVa is an aldol condensation with a glyoxalic acid derivative, generally a lower alkyl ester. The

reaction is catalyzed by acids or bases, e.g. preferably metal alkoxides. It is preferably conducted in an inert atmosphere, e.g. nitrogen, at a temperature of from about 80-120 C. for from /4 to about 24 hours using from about A; to 2.0 moles metal ion/mole of triketone. The acid catalyzed condensation is conveniently carried out in glacial acetic acid as solvent. Non-hydroxylic solvents such as benzene, xylene, toluene, dioxane, dimethoxyethane, diethyleneglycoldimethylether and dimethylformamide are useful solvents for the metal catalyzed condensation, especially when using metal alkoxides. Magnesium methoxide is especially useful in this condensation. Of course, when active hydrogen (in addition to that of the ,B-diketone system) is present, one extra equivalent of alkoxide is used per active hydrogen. The a-hydroxy ester, wherein the elements of water are added to the unsaturated ester, is also obtained in small yield. Its production is favored by short reaction periods and low temperatures. Dehydrating agents, such as phosphorous oxychloride in pyridine at 0 C. and p-toluenesulfonic acid in benzene permit dehydration and generation of the unsaturation.

The conversion of XVa to XV is a Michael reaction with an amine HNR R The reaction is conducted at a temperature of from about 70 C. to about C. preferably at about C. An excess of the amine is employed; a sufficiently large excess frequently being used to serve both as solvent and as reactant. A variety of other solvents can be used and are actually necessary when the amine is a solid at the temperature of the reaction. Such solvents include tetrahydrofuran, ethylene glycol ethers, diethyleneglycol ethers and chloroform. The only criteria essential for the solvent are adequate solubility for the reactants, inertness and a sufliciently low freezing point.

The reaction is run for periods of from 15 minutes to 24 hours depending upon the reactants and temperature employed. Oxygen should be excluded during the period When the product is in contact with the excess amine. The order of addition of the reactants appears, in general, to be immaterial to the outcome of the reaction.

In some instances the ester group is transformed to the amide corresponding to the amine reactant. Primary lower alkylamines may also enter into further reaction involving the 3-keto group. This appears to be a transient or intermediate step in the reaction and, as long as the amine addition product is retained in solution, can be directly reduced to the 3-hydroxy amino acid ester (XVb). Isolation of the amine addition product, however, produces what is believed to be a fused lactam possibly via formation of a hydroxy amine at the 3-position followed by elimination of alcohol between the ester and amine groups.

From XV to XVb is a selective reduction with a suitable chemical reducing agent, such as metal hydrides, especially sodium borohydride. The reaction is carried out by dissolving the amino acid ester reactant in a suitable reactioninert solvent such as 1,2-dimethoxyethane, ethylene-glycol ethers, diethyleneglycol ethers and liquid amines. When hydroxylic solvents are employed, e.g. alcohols, an excess of sodium borohydride is used. Reaction periods of from about 10 minutes to about 3 hours are required. Of course, when active hydrogen is present in the reactants, one equivalent of sodium borohydride is required per active hydrogen in addition to that of the B-diketone system.

Alternatively, the reduction is conducted by adding the sodium borohydride all at once to a vigorously stirred solution of the amino acid ester (XV) in one of the aforementioned solvents at 70 C. followed by gradual increase in the temperature to 0 C. In this process, as above, 0.5 to 4.0 moles of reducing agent per mole of amino acid ester is used. A ratio of 1 is, however, preferred (except in cases where active hydrogen is present).

From XVa to XVb is a selective reduction with a suitable chemical reducing agent, such as sodium borohydride, of the Mannich reaction product XV. It is represented as a one-step conversion since the Michael reaction product need not be separated prior to reduction. Simultaneous formation of the corresponding lactone also occurs.

The lactone, of course, serves as a suitable reactant for the production of XVb by cleavage of the lactone ring under mild conditions.

The formation of XIX from XVIII (RFH) is accomplished by formation of a mixed anhydride (R =CO X with a haloalkyl carbonate as described in the I. Am. Chem. Soc. 75, 6369 (1953) and the J. Org. Chem. 22, 248 (1957). Acylation of a malonic acid ester derivative, e.g., malonic diester, cyanoacetic ester, malonic ester half amide, including N-alkylated amides and especially the magnesium salt of ethyl t-butyl-malonamate etc., with the mixed anhydride produces the corresponding malonic acid derivative. Reaction is conducted in a suitable solvent system such as chloroform, toluene, benzene, diethylether, acetonitrile, dimethylformamide, nitromethane, dioxane, tetrahydrofuran, ethers of ethyleneglycol and diethyleneglycol at from about 5 to about 35 C. for periods ranging from 25 minutes to up to 3 days. When R is CO X the malonic acid derivative is employed as a magnesium enolate according to the procedure of Tarbell and Price (J. Org. Chem., loc. cit.).

Where X is CONH-alkyl, e.g. t-butyl or isopropyl carboxamido, treatment with concentrated sulfuric acid yields the corresponding unsubstituted carboxamide.

The conversion of XIX to XVII is accomplished by standard base-catalyzed acylation using, for example, sodium alkoxides, sodamide or preferably sodium hydride. A ratio of at least 4 equivalents of base and desirably a great excess of up to 10 equivalents is employed. A variety of reaction-inert solvents can be used, eg benzene, xylene, toluene, anisole, dimethylformamide. Dimethylformamide containing a small amount of methanol is the preferred solvent. Reaction is conducted under nitrogen at a temperature of from about to about 150 C. preferably C., for periods of from about 3 minutes to up to 24 hours depending upon the reactants. A period of 57 minutes is adequate, indeed preferred, in most instances. When Y CN, the 12-imido group which results is hydrolyzed with aqueous acid to the 12-keto group.

The compounds of structures XVI and XVII in which X, is a carboxamide group are biologically active tetracycline products, the latter being 12a-deoxytetracyclines which are converted to tetracycline compounds XVI by introduction of a 12a-hydroxy group by known procedures such as described in the J. Am. Chem. Soc., 81, 4748 (1959).

A preferred method of IZa-hydroxylation is the method described in U.S. Patent 3,188,348, issued June 8, 1965, wherein is described the hydroxylation of certain metal chelates of the 12a-deoxytetracyclines. The advantage of this latter process lies in the fact that the hydroxy group is introduced cisto the hydrogen at position 4a.

Compounds of structures XVI and XVII in which X, is a cyano group are converted to corresponding carboxamido substituted compounds by the method described in U.S. Patent 3,029,284, issued Apr. 10, 1962 wherein is described the conversion of tetracycline nitriles to the corresponding carboxamide by the Ritter Reaction followed by dealkylation of the resulting N-alkylated carboxamide with concentrated mineral acid and water.

The diketo compound XVIII is obtained from the hydrochloride of XVb via the lactone by treatment with from about 0.5 to about 2 equivalents of p-toluenesulfonic acid in a suitable reaction-inert solvent (benzene, toluene, xylene) for periods of from about 5 hours to about 2 days. A temperature of from about 80-140 C. is satisfactory. The lactone hydrochloride of XVb is then treated with zinc dust-formic acid for a brief period to give XVIII wherein R is hydrogen. A ratio of from 1 to 20 equivalents of zinc dust is effective in cleaving the lactone to the free acid; 67 equivalents are preferred. Formic acid is the solvent of choice. However, mixtures of formic acid-methanol-water or of acetic acid-methanol-water, in approximately 1:1:1 ratio, can also be used. A temperature of about 25 C. is generally used, although this is not a critical level. To avoid reduction of the 4,.l-diketo system, it is important that mild reaction conditions and brief contact times be employed. Contact times of from about 30 seconds to several hours depending upon the reactants, are operative. In general, however, periods of from 45 seconds to 120 seconds are favored.

Alternatively, conversion of XVb to the diketo compound XVIII (X =CH is accomplished by reaction with acetoformic anhydride according to known procedures followed by removal of the 3-formyloxy group by one of the following; treatment with zinc dust-formic acid or zinc dust in aqueous ammonium hydroxide, calcium in liquid ammonia, or catalytic hydrogenation (5% Pd-C) in tetrahydrofuran or formic acid. Care must be taken to avoid over-reduction, that is, reduction of the 4,10-keto group. For this reason mild conditions are required. When using zinc dust-formic acid, for example, reaction is effected at room temperature with contact times of brief duration.

The 8-chloro atom of the diketo octahydroanthracene amino acid (XVIII, X CH and R H), corresponding to the 7-chloro atom of the final tetracycline products can, if desired, be readily removed by catalytic hydrogenolysis. Pd-C or Pt-C containing 5-l0% of the metal are most elfective for this purpose. Pd-C is preferred. From about 0.1 to 1 weight equivalent is used. Dimethylformamide, tetrahydrofuran, water, ethanol and ethylacetate, preferably ethanol, serve as solvents. Pressures of from about 1 atmosphere to high pressures, e.g. 70 atmospheres or higher, and temperatures of from -20 C. to 60 C. or higher can be used. The preferred conditions are atmospheric pressure and room temperature for periods of about 3 hours. A base is required to take up the hydrogen chloride produced. While a variety of bases, both organic and inorganic by nature, can be used, it is preferred to use triethylamine, generally about 4 equivalents.

When the substituents of the present compounds are hydroxy or amino, the use of a blocking group is sometimes advantageous in obtaining high yields during their preparation. Especially useful blocking groups are acyl, benzyl, tetrahydropyranyl, methoxymethyl, methyl and ethyl radicals. Benzyl ethers are particularly easily reduced to hydroxyl groups. Tetrahydropyranyl ethers are easily removed under mildly acidic conditions. Acyl groups which may be used include the acetyl, propionyl and butyryl, as well as the benzoyl, succinyl, phthaloyl, and the like. The lower alkyl blocking groups are preferred since these compounds are readily prepared.

When desired the above mentioned blocking groups, i.e., enol ether radicals, may be removed. The enol radicals are hydrolyzed by treatment with aqueous acid as is well known by those skilled in the art. When the ether radical is benzyl, hydrogenolysis over noble metal catalyst may also be used.

In compounds of Formula XVII, for example, the compound wherein X, X; and A are hydrogen; X is 10- methoxy; R and R are methyl and X is N-t-butylcarboxamido, the IO-methyl ether and the t-butyl group at the 2-position are conveniently removed in a single step by treatment with 48% HBr for up to minutes at about 100 C. If shorter periods of time, e.g. 5 minutes, are used only the 10 methyl ether may be cleaved. Alternatively, the protective methyl and t-butyl groups can be removed in stepwise fashion. Treatment with 85% H 50 for 2 hours at about room temperature removes only the t-butyl group to give the Ill-methyl ether of 6-demethyl- 6,lZa-dideoxytetracycline. The 10 methyl group is then 8 removed by treatment with 48% HBr, or with hot concentrated HCl, or hot 50% H SO The new compounds described herein are useful as chelating, complexing or sequestering agents. The complexes formed with polyvalent metal ions are particularly stable and usually quite soluble in various organic solvents. These properties, of course, render them useful for a variety of purposes wherein metal ion contamination presents a problem; e.g. stabilizers in various organic systems, such as saturated and unsaturated lubricating oils and hydrocarbons, fatty acids and waxes, wherein transition metal ion contamination accelerates oxidative deterioration and color formation, biological experimentation, metal extraction. They are further use ful in analysis of polyvalent metal ions which may be complexed or extracted by these materials and as metal carriers. Other uses common to sequestering agents are also apparent for these compounds.

In addition, the compounds of Flow Sheet I are especially valuable as intermediates in chemical synthesis particularly in the synthesis of fi-deoxytetracycline, 6-deoxyfi-demethyltetracycline and other novel antimicrobial agents bearing structural similarities to the tetracycline antibiotics. Many of the herein described compounds, especially those containing one or more hydroxy groups in the benzenoid moiety, are useful as antibacterial agents in their own right.

In the present new process, particularly as applied to the synthesis of biologically active tetracyclines, it is preferred to employ intermediates in which the hydrogen atoms at the 9a and 2-positions of the anthracene ring (corresponding to the 4a and Sa-positions of the tetracycline nucleus) are in the cis arrangement. For example, preferred compounds are depicted by the following formula (syn compounds):

In general, syn and anti compounds are separable by virtue of differences in physical properties, e.g. differences in solubility in various solvents. Usually, fractional crystallization permits ready separation.

It is a particular advantage of the novel triketo octahydroanthracenes of the present inventiton that, by virtue of the activating influence of the carbonyl oxygen, they equilibrate to the predominately cis configuration in the course of preparation. This enables the synthesis to proceed in stereo-specific fashion without the loss of material that would otherwise be entailed in the separation of syn and anti compounds.

However, since in the production of compounds of this type, the product may consist of a mixture comprised of compounds differing in position of the anthracene nucleus, i.e. the hydrogen being both cis and trans to the hydrogen at position 9a, the mixture can be converted to the predominately cis arrangement by equilibration in aqueous alkali, e.g. by treatment with aqueous sodium hydroxide or under the influence of the amine in the Mannich reaction. The procedure merely involves dissolving the reaction produ-ct in aqueous base and allowing the mixture to stand for periods of several hours 9 to ensure complete equilibration. In lieu of this procedure, equilibration is attained via the Michael reaction using extended reaction periods.

It is recognized by those in the art that, when such compounds have an asymmetric center in the substituent G, they exist as diastereoisomers which, as previously mentioned, may be separated by fractional crystallization for each of the syn and anti compounds. Of course, as is known, diastereoisomers are racemic modifications consisting of two structures which are mirror images (optical antipodes). The racemic modifications may be resolved according to standard procedures. In the present process it is preferred, however, to utilize the diastereoisomers of the syn compounds since changes in configuration may occur during the various procedural steps of the total synthesis to tetracycline compounds, thus necessitating costly and time-consuming resolution procedures. The syn diastereoisomers are converted to tetracycline products which consist of the normal tetracyclines and their 4-epimers which are separable by known procedures. Of course, the 4-epitetracyclines are useful in that they are converted to normal tetracyclines by known procedures.

The starting compounds of structure I are prepared according to the following procedure:

CORs

Xl I 2 II ll in the abnve formulae, X, X X and A are as previously described with the exception that substituent X is preferably not a nitro group since this group deactivates the ring of compounds of structure II in the ring closure reaction to those of structure III; (R is lower alkyl or benzyl) and R is hydroxyl, benzyloxy, lower alkoxy or halogen (Cl, F, Br, or 1). Alternatively, the corresponding nitriles (e.g. where COR is replaced by CN) may be used. Further, at least one of the two positions of the benzenoid ring ortho to the diester side chain must be available for the ring closure of structure II compounds. If desired, halogen, (C1 or Br) may be introduced into compounds of structure I, II, III and IV in which at least one of the benzenoid substituents is hydrogen by direct halo genation with a chlorinating or brominating agent by methods generally employed for halogenation of an aromatic ring. A variety of such agents are known to those in the art and include phosphorus pentachloride and pentabromide, sulfuryl chloride, N-chloro or bromoalkanoamides, e.g. N-chlorand N-bromoacetamide; N-chloro (or bromo) alkanedioic acid imides, e.g. N-halosuccinimide; N-halophthalimide; chlorine; bromine; N-halolwhere R2=OR1 acylanilides, e.g. N-bromoacetanilide, propionanilide and the like; 3-chloro, 3-bromo, 3,5-dichloro and 3,5-dibromo 5,5-dimethylhydantoin; pyridinium perbromide and perchloride hydrohalides, e.g. pyridinium perbromide hydrobromide; and lower alkyl hypochlorites, e.g. tertiary butyl hypochlorite.

Of particular value are compounds of the following formula:

Xl A H OOR X I 0R5 OR IID through the sequences represented by II III- IV I and II VI IV- I. In the ring closure reaction of corresponding structure II compounds, it is preferred that the henzenoid substituent (X para to substituent OR be other than hydrogen to enable the ring closure reaction to proceed in the position ortho to substituent OR to afford corresponding structure III compounds. If there is no substituent para to OR a halogen group may be introduced by direct halogenation by conventional methods as hereinbefore described. The para halogen substituent may be removed, if desired, by hydrogenolysis, under the usual conditions, of the tetralone resulting from the ring closure.

The ring closure of compounds II to III is accomplished by any of the commonly employed methods for such reactions which generally involve the use of a dehydrating or dehydrohalogenating cyclization agent. With compounds of structure 11, a preferred method when R is OH or alkoxy, involves treatment of the starting compound with such ring closure agents as hydrogen fluoride or polyphosphoric acid. When R in the starting compound is hydroxyl, it is usually preferred to use hydrogen fluoride; when R is lower alkoxy, polyphosphoric acid. When R is halogen a Friedel-Crafts catalyst, of course, should be employed, e.g. aluminum chloride. m-Hydroxyor alkoxybenzyl compounds of structure II having ON in place of COR lend themselves to the Hoesch synthesis (Berichte, 48, 1122 and 50, 462) wherein treatment with dry hydrogen chloride in the presence of Zinc chloride leads to imine formation, and hydrolysis of the latter provides the tetralone keto group.

The condensation of compounds II or III in which R is 0R with oxalic ester as well as ring closure of compounds IIIa (after esterification of the free acid with R OH) are effected by the general methods for ester condensation reactions of this type. Usually the reaction is carried out in the presence of a strong base such as alkali metal, alkali metal alkoxides and hydrides, sodamide and the like. If the starting compound in the oxalate condensation contains free hydroxyl, or amino groups it is preferred to block uch group by alkylation or acylation by known procedures. After the reaction is completed, the blocking groups may be removed, if desired. The resulting product from structure II, i.e. the corresponding 2-carbalkoxy or carbobenzyloxy compound of structure IV, on hydrolysis and decarboxylation yields compounds of structure I; structure VI compounds are first ring closed, e.g. with polyphosphoric acid and then hydrolyzed and decarboxylated to those of structure I. Cleavage of the ether linkage or other blocking groups by any of the general methods, e.g. treatment with mineral acid such as concentrated hydrobromic or hydriodic acid, or when R is benzyl, hydrogenolysis, gives free hydroxy groups in the benzenoid portion.

The starting compounds of the above described processes, i.e. compounds of structure II, are prepared by the following sequences of reactions.

X flu WFC Hal In the above sequence, R and R are lower alkyl or benzyl; and B is hydrogen or hydroxy. Further, in this sequence a lower alkyl group can be present in the starting diether at the 4-position of the aromatic ring, if desired, to produce 3-benzyl-4-(lower alkyl) substituted adipic acid derivatives (II).

FLOW SHEET II The first of these reactions for the preparation of compounds of structure VII is by means of Friedel-Crafts reaction, e.g. AlCl in carbon disulfide. The conversion of compounds of structure VII to those of VIII in which A and B are hydrogen is by catalytic reduction, e.g. over copper chromium oxide or noble metal, e.g. palladium, catalyst at from atmosphere to superat-mospheric pressures of hydrogen gas; where A is alkyl and B hydroxyl, by reaction with a suitable Grignard reagent, e.g. AMgHalogen; where A is alkyl or hydrogen and B is hydrogen, by reduction, i.e. hydrogenolysis, of corresponding compounds in which E is hydroxyl. From VIII to IX is a standard ether hydrolysis, e.g. concentrated hydrobromic acid.

From IX to X is an ozonolysis reaction giving rise to the dienedioc acid which on hydrogenation over a noble metal catalyst, e.g. palladium, palladium on carbon, platinum, platinum oxide, etc., gives compounds of structure II. In the ozonolysis reactions to form compounds of structure X it is not possible to employ as starting compounds those of structure IX in which there are adjacent hydroxyl groups in the benzene ring containing X, X, and X as substituents, since such structures are susceptible to the oxidation reaction.

Further, in the ozonolysis reaction compounds of structure IX in which X, X and X are adjacent ether groups or adjacent ether and hydroxy groups cannot be used since they, too, are susceptible of oxidation. The ozonolysis reaction is applicable to compounds of structures VIII, subject of course to the above limitation, wherein 0R represents an ether group. In such cases the ester (X) is obtained. In the hydrogenation reaction, compounds of structure X may be used as the free acids or corresponding benzyl or lower alkyl esters to provide corresponding products of structure II. Of course, benzyl esters may undergo hydrogenolysis to the free acid.

In addition, appropriate methods are available for reduction of the benzoyl keto group to a secondary alcohol. For example, 1111 and VII can be reduced with sodium borohydride, or by hydrogenation with palladium catalyst in non-acidic media. By other well-known replacement procedures such as the following, the secondary alcohol may be converted to a readily replaceable sulfonic ester group, e.g. the tosylate, mesylate, etc., followed by reaction with an alkali metal cyanide, an amine, a malonic ester, or the like, thus affording means for introduction of a cyano, amino or CH(CO B group in the 6-position of the final tetracycline. The secondary alcohol can also be dehydrated and the resulting unsaturated compound reduced to the corresponding benzyl derivative.

In this sequence of reactions, when X and/or X are halogen, care should be taken to avoid prolonged hydrogenations which may result in the removal of the halogen atom. The possibility of halogen removal may be minimized by the use of a lower alkanoic acid, e.g. acetic or propionic as solvent for the reaction. Of course, it removed, halogen may be reintroduced if desired by the method hereinbefore described.

In those compounds of structure IX in which there are adjacent hydroxy groups in the benzenoid moiety, such groups must be protected by suitable blocking groups, e.g. etherified with lower alkyl or benzyl groups. Similarly, free amino groups maybe acylated. Of course, the etherifying radical of the hydroxy group may diifer from that represented by R. If the etherifying radical is benzyl it may subsequently be removed by hydrogenolysis. Alternatively, all ether groups can be removed by hydrogen iodide treatment.

As will be appreciated from the preceding reaction sequence, it is most convenient to introduce the benzenoid substituents, X, X; and X by employing the appropriately substituted benzoic acid derivative as starting material. Many of these benzoic acid derivatives are commercially available, and others may be readily obtained by those skilled in the art.

It will be noted that a number of the later steps of the preceding sequences involve reaction conditions which may affect certain of the substituent groups signified by X, X and X For instance, in catalytic hydrogenation; e.g. VIIVIII, halo groups are subject to hydrogenolysis. Therefore, where halo groups are desired in the final product, these are best introduced subsequent to the hydrogenation by an appropriate substitution reaction.

In commencing the sequence with a substituted benzoyl succinate, it is essential that an ortho ring position be unsubstituted, since cyclization to form the center ring of the hydroanthracene occurs at this position. For the preparation of the preferred compounds of structure I, which bear an OR substituent in the 5-position, the position of the benzene ring between the OR group and the keto group in the starting benzoyl succinate should be unsubstituted, to provide for the subsequent ring closure. On the other hand, it is preferred to have a substituent in what corresponds to the 8-position of compound 1, since this precludes cyclization to that position in competition with the desired cyclization [II- 111]. A CF alkyl, or acylamino group can be conveniently carried in this position from the outset. Alternatively, an 8-substituent may be introduced during the reaction sequence, prior tothe 13 cyclization. For example, compound II may be halogenated at this position, e.g. by treatment with chlorine in the presence of a catalytic amount of iodine or ferric chloride.

Compounds of structure II are also prepared by the following sequences of reactions.

X2 CO2R1 O A COzRi X X1 COzRi XII CO2R 002111 X I X H X1 X1 COzRi X2 X2 XI XIV COzR X H XIII The conversion of compounds of Formula XI to those of XII is a Claisen-type condensation of the lower alkyl ester of XI with succinic acid diesters to provide Formula XII compounds. The conversion of compounds of Formula XI to XIII is similarly a Claisen condensation using acetic acid esters. The conversion of compounds of Formula XIII to XII is by alkylation reaction with a monohaloacetic 5O acid ester, and the conversion of XIV to 11a is such an alkylation followed by hydrolysis and decarboxylation. The preparation of compounds of Formula XIV from those of Formula XIII is by standard alkylation procedures preferably using H C=CHCO R or corresponding nitriles. This conversion may also be effected by alkylation with a B-halo acid derivative halogen-CH CH CO R or the corresponding nitrile. Each of these reactions are effected under standard conditions known to those skilled in the art, e.g. in a reaction-inert solvent in the presence of a base such as Triton B (benzyltrimethylammonium hydroxide), sodamide, sodium hydride and their obvious equivalents.

The conversion of compounds of Formula XII to those of .IIa is by known standard reactions, e.g. by reaction of Formula XII compounds with corresponding acrylic acid esters of the formula H C=CHCO R in which A and R are as previously described under the conditions of the Michael reaction. It may also be effected by alkylation with ,B-halo-alkanoic acids of the formula Halogen-CH CH CO R or of the corresponding nitriles. Hydrolysis and decarboxylation of these compounds gives structure IIa compounds. The conversion of structure Ila compounds to those of structure II is brought about by reactions as 7 previously described for preparing structure VIII compounds.

The present invention additionally is adaptable for the preparation of other tetracycline molecules, as follows.

For compounds in which substituent X is nitro, the tetralone of structure III is nitrated by standard procedures, e.g., such as nitric-acetic anhydride-acetic acid mixtures or nitric acid-sulfuric acid mixtures. Those in which X is halogen, cyano, nitro or other such groups are prepared by a Sandmeyer reaction of the corresponding diazonium salt with suitable salt reagents (Cu Cl -Cu Br KI, etc.). The diazonium salt is obtained by diazotization of the amino compound, prepared from compounds of structure 11 in which X is amino or produced by the reduction of the corresponding nitro compound by conventinal means, e.g., chemical means, such as, active metals (Sn) and mineral acids (HCl) or by catalytic hydrogenation, e.g., nickel catalyst and superatmospheric pressure.

The amino group may also be introduced into the ben- Zenoid ring by coupling of aryldiazonium salts, e.g., benzene diazonium chloride or the diazonium salt of p-aminobenzenesulfonic acid, with compounds of structure II or III containing a free hydroxy substituent in the 5-position of the 4-tetralone ring (3-position of the benzene ring) followed by reduction of the resulting phenylazo compound, e.g., catalytic reduction over noble metal catalysts. An amino group may also be introduced in place of the keto carbonyl oxygen of compounds of structure VII and XIV by reduction of the corresponding oxime or hydrazone, by reductive ammonolysis of the keto carbonyl group over noble metal catalysts or by reduction of the keto group to a secondary hydroxy group by sodium borohydride followed by conversion to the tosylate and replacement of the tosylate group by an amino group.

A further modification of the present invention provides a means of introducing a variety of substituents in positions corresponding to the 5a, and 6-positions of the tetracycline nucleus. This involves formation of the secondary alcohol corresponding to structure IIA compounds represented by the formula:

COzR1 IIb by partial reduction of the corresponding ketone over palladium catalyst at superatmospheric pressure until only one molar equivalent of hydrogen is taken up. Compounds of structure 1112 are also intermediates for the preparation of 6-demethyltetracyclines.

The benzoyl keto group of compounds of structure Ila may be subjected to the Wittig reaction as described in Angewandte Chemie 71, 260-273 (1959) to produce the alkylidene derivatives He by treatment with the ylid prepared from a chloroether of the formula (B )CHClOB (where B is lower alkyl and B is hydrogen or lower alkyl) The necessary chloroethers are obtained by standard treatment of aldehyde acetals of the formula (B )CH(OB with an acid chloride (J. Org. Chem. 231, 1936).

Treatment of compounds Ila in this fashion with the ylid from chloromethyl ether, for example, converts the keto group to a methoxy-methylene group, which may be reduced to methoxymethyl. The latter group may be carried through the subsequent steps herein described to the 6-methoxymethyltetracycline. At this point the elements of methanol may be split out by standard pro cedures to obtain the 6-methylene-fi-deoxy-d-demethyltetracycline.

The products of the above reaction may, in turn, be hydrogenated with noble metal catalysts:

B (B B OCH(B 2 a) C0231 2 a 002R subjecting the reduction products to the further synthetic sequences illustrated herein yields tetracyclines having a 6-CH(B 0B substituent. Treatment of such tetracyclines with liquid hydrogen fluoride results in the elimination of a mole of alcohol B OH and provides tetracyclines having a =CH(B at the 6-position. The latter treatment is, for example, conveniently effected after the introduction of the lla-hydroxyl group. Alternatively, treatment of such tetracyclines having a 6-CH(B )OB group converts this group to CH(B )OH with concurrent hydrolysis of any ether groups in the aromatic D-ring.

The products of the Wittig reaction IIC may also be hydrolyzed to aldehydes and the resulting aldehyde group inturn converted by catalytic hydrogenation to a hydroxy methyl group. The latter may be carried through the subsequent reactions of synthetic sequence with its free hydroxyl group, or preferably, in the form of a lower alkyl ether.

The described procedures are adaptable to the preparation of a variety of tetracycline molecules, as follows:

For introduction of aromatic nitro groups, the given compound, e.g. tetralone III, is nitrated by standard procedures, such as treatment with nitric acid-acetic anhydride-acetic acid mixtures, or nitric-sulfuric acid mixtures. Those in which X is halogen, cyano, halo sulfonyl nitro or other such groups may be prepared by Sandmeyer reaction of the corresponding diazonium salt with suitable salt reagents (Cu Cl Cu Br etc.). The diazonium salt is obtained by diazotization of the amino compound, which may in turn be prepared by reduction of the corresponding nitro compound by conventional means, e.g. chemical reduction with active metals (Sn) and mineral acids (HCl) or catalytic hydrogenation, e.g. with nickel catalyst at superatmospheric pressure. Aromatic cyano groups may be further converted. to carboxy or carbalkoxy groups where desired by standard hydrolysis and esterification.

The amino group may also be introduced into the benzenoid ring, e.g. in compounds of structure II having a phenolic hydroxyl group, by coupling with aryldiazonium salts such as benzene diazonium chloride or the diazonium salt of p-aminobenzenesulfonic acid, followed by reduction of the resulting phenylazo compound, e.g. by catalytic hydrogenolysis with noble metal catalysts.

As has been previously pointed out, normal discretion must be employed in subjecting certain of the substituted intermediates to the herein described reaction steps. In the base condensation reactions, the presence of a substituent having an active hydrogen (e.g. a hydroxyl, or amino group) will necessitate the use of an additional mole of the sodium hydride or other base. The presence of more than one such substituent per molecule is preferably avoided in these reactions, e.g. by the use of protective ether groups as previously described. The same considerations apply to Grignard reactions and hydride reductions. Hydroxyl groups can be subsequently regenerated from their ethers by conventional hydrolytic procedures such as treatment With hydrogen bromide. Similarly, protective benzyl ether groups can subsequently be hydrogenolyzed to obtain hydroxyl groups where desired.

In the reduction of benzoyl adipate Ila or benzophenone VII to the corresponding benzyl derivatives II and VIII, chemical reduction with amalgamated zinc and HCl by the well-known Clemmensen procedure may be employed in place of catalytic hydrogenolysis. Any ester groups which may be present in the molecule are concurrently hydrolyzed in the Clemmensen procedure, and reesterification will therefore be necessary.

Alternative routes or procedures can be used in place of the Clemmensen reduction. Thus, in the reduction of benzoyl adipate 11a to corresponding benzyl derivative II, the three-step procedure previously referred to is an appropriate alternative to direct reduction; ie (1) conversion of the keto group to hydroxyl, e.g. with sodium borohydride or by mild reduction at room temperature with palladium on carbon in alcohol or other neutral solvent; (2) conversion of the resulting alcohol to the unsaturated compound by dehydration in anhydrous hydrogen fluoride; and (3) rapid hydrogenation of the re sulting double bond, e.g. with palladium at room temperature and moderate hydrogen pressure, until one mole of hydrogen has been consumed. Another alternative reduction procedure which is suitable is the Wolf-Kishner reaction (Annalen, 394, 90, 1912 and 1. Russ. Phys. Chem. Soc. 43, 582, 1911) wherein the benzoyl derivative is converted to a hydrazone, and the latter is in turn reduced to the corresponding benzyl derivative by heating with a base such as sodium ethoxide.

The present invention provides a means of synthesizing tetracycline compounds including 8-substituted and other valuable new tetracyclines, not previously described, which are therapeutically useful by virtue of their antimicrobial activity.

Those skilled in the art will appreciate that the following examples provide a basis for preparing the listed tetracyclines and the corresponding 12a-deoxy derivatives thereof.

Of particular significance in accordance with this invention are those final tetracycline products (XVI and.

XVII) wherein a hydroxy group or a group readily convertible to a hydroxy group (alkoxy or alkanoyloxy) is present at the 8position. An additional substituent of importance in accordance with this invention is the trifluoromethyl group when present at the 7- and or 8-p0sitions of the final tetracyclines.

Some of the new tetracyclines of the present invention are homologs, isomers or closely related analogs of known tetracyclines. Many of the new tetracyclines are distinguished from prior art compounds by their possession of important and desirable properties, such as extended in vitro and in vivo antibacterial spectra, activity against organisms which have inherent or acquired resistance to known antibiotics, rapid absorption, sustained blood levels, freedom from serum binding, preferential tissue distribution at various parts of the body (e.g. kidney, lung, bladder, skin, etc.) which are sites for infection, sustained stability in a variety of dosage forms, resistance to metabolic destruction, broad solubility, and freedom from objectionable acute and cumulative sideetfe-cts. The new tetracyclines are useful in therapy, in agriculture, and in veterinary practice both therapeutically and as growth stimulants. In addition, they may be employed as disinfectants and bacteriostatic agents, in industrial fermentations to prevent contamination by sensitive organisms, and in tissue culture, e.g. for vaccine production.

The various new tetracyclines of the present invention which do not share the antibacterial activity of the known tetracyclines are valuable intermediates in the preparation of other compounds of classes known to contain biologically active members. Thus, the D-ring can be nitrated directly and the nitro derivative reduced catalytically to an aminotetracycline. Further, the tetracycline products of this invention can be halogenated by known methods at the 1la-, or in the case of a 7-unsubstituted tetracycline, in the 7,11a-positions by treatment with such halogenating agents as perchloryl fluoride, N-chlorsuccinimide, N-bromsuccinimide and iodobromide.

The present invention embraces all salts, including acidaddition and metal salts, of the new antibiotics. Such salts are formed by well known procedures with both pharmaceutically acceptable and pharmaceutically unacceptable acids and metals. By pharmaceutically acceptable is meant those salt-forming acids and metals which do not substantially increase the toxicity of the antibiotic.

The pharmaceutically acceptable acid addition salts are of particular value in therapy. These include salts of mineral acids such as hydrochloric, hydriodic, hydrobromic, phosphoric, metaphosphoric, nitric and sulfuric acids, as well as salts of organic acids such as tartaric, acetic, citric, rnalic, benzoic, glycollic, gluconic, gulonic, succinic, arylsulfonic, e.g. p-toluenesulfonic acids, and the like. The pharmaceutically unacceptable acid addition salts, while not useful for therapy, are valuable for isolation and purification of the new substances. Further, they are useful for the preparation of pharmaceutically acceptable salts. Of this group, the more common salts include those formed with hydrofluoric and perchloric acids. Hydrofluoride salts are particularly useful for the preparation of the pharmaceutically acceptable salts, e.g. the hydrochlorides, by solution in hydrochloric acid and crystallization of the hydrochloride salt formed. The perchloric acid salts are useful for purification and crystallization of the new products.

Whereas all metal salts may be prepared and are useful for various purposes, the pharmaceutically acceptable metal salts are particularly valuable because of their utility in therapy. The pharmaceutically acceptable metals include more commonly sodium, potassium and alkaline earth metals of atomic number up to and including 20, i.e., magnesium and calcium and additionally, aluminum, zinc, iron and manganese, among others. Of course, the metal salts include complex salts, i.e. metal chelates, which are well recognized in the tetracycline art. The pharmaceutically unacceptable metal salts embrace most commonly salts of lithium and of alkaline earth metals of atomic number greater than 20, i.e., barium and strontium, which are useful for isolating and purifying the compounds.

It will be obvious that, in addition to their value in therapy, the pharmaceutically acceptable acid and metal salts are also useful in isolation and purification.

The new tricyclic intermediates of the present inven tion, in addition to their value in synthesis, exhibit valuable antimicrobial activity. They may be employed as bacteriostatic agents, and are further useful in separation and classification of organisms for medical and diagnostic purposes. These new intermediates, by virtue of their 8- diketone structure, are also valuable chelating, complexing or sequestering agents, and form particularly stable and soluble complexes with polyvalent cations. They are therefore useful wherever removal of such polyvalent ions is desired, e.g., in biological experimentation and in analytical procedures. Of course, as is well known to those skilled in the art, such fl-diketones may exist in one or more of several tautomeric forms as a result of their ability to enolize. It is fully intended that the B- diketone structures herein employed embrace such tautomers.

The starting compounds of the present invention are readily preparable by known procedures. Many of these compounds, including both benzoic acid esters and benzophenone starting compounds, have been described in the literature.

The following examples are given by way of illustration.

EXAMPLE I Monoethyl ester of 3-(3-methoxybenzyl)adipic acid Method A.Five grams of diethyl 3-(3-methoxybenzoyl)adipate and 2 g. of 5% palladium on carbon in 30 ml. of acetic acid are treated in a conventional Parr shaker at a pressure of 40 p.s.i. of hydrogen gas at 50 C. until 2 moles of hydrogen are taken up. The first mole of gas is taken up rapidly and the second more slowly over a total reaction time of up to about 30 hours. The mixture is filtered, concentrated under reduced pressure to an oil which is vacuum-distilled to obtain the product.

Method B.The -lactone of the enol form of the monoethyl ester of the starting compound is hydrogenated over palladium on carbon by this same method to obtain this product, B.P. 1901 (0.3 mm.). Elemental analysis gives the following results:

Calcd. for C H O (percent): C, 65.29; H, 7.53. Found (percent): C, 65.25; H, 7.68.

The corresponding diethyl ester is prepared by refluxing this product in ethylene dichloride containing ethanol and sulfuric acid. The diester is obtained by diluting the reaction mixture with water, separating, drying and concentrating the ethylene dichloride layer, and vacuum-distilling the residual oil, n =l.4973. Elemental analysis gives the following results:

Calcd. for C H O (percent): C, 67.06; H, 8.13. Found (percent): C, 67.02; H, 8.31.

The starting compound together with the corresponding 'y-lactone are prepared by hydrolysis and decarboxylation of diethyl 3-carbo-t butoxy-3-(3-methoxybenzoyl)adipate (Example XLV) by refluxing in dry xylene containing ptoluenesulfonic acid. The products are separated by fractional distillation or may be used together as starting compound for this hydrogenation reaction.

EXAMPLE II 3- 3-methoxybenzyl) adipic acid Method A.Amalgamated zinc is prepared by shaking for 5 minutes a mixture of 120 g. of mossy zinc, 12 g. of mercuric chloride, 200 ml. of water and 5 ml. of concentrated HCl. in a round-bottomed flask. The solution is decanted and the following reagents added: ml. of water and 175 ml. of cone. HCl, ml. of toluene and 52 g. of 3-(3-methoxybenzoyl)adipic acid. The reaction mixture is vigorously boiled under reflux for 24 hours. Three 50 ml. portions of concentrated HCl are added at intervals of 6 hours during reflux.

After cooling to room temperature, the layers are separated, the aqueous layer diluted with 200 ml. of water and extracted with ether. The ether extract is combined with the toluene layer, dried and concentrated under reduced pressure to obtain the product.

Method B.A solution of 6254.4 grams (22.1 mole) 3-(3-methoxybenzoyl)-adipic acid in 38.5 liters of glacial acetic acid is hydrogenated in a 15 gal. stirred autoclave in the presence of 2.5 kg. 5 percent palladium-on-carbon catalyst at 1000 p.s.iig. and 50 C. until the theoretical amount of hydrogen has been absorbed. The catalyst is filtered off and the solvent removed from the filtrate by distillation at reduced pressure. This gives 5432 grams of product in the form of an oil. It is further purified by conversion to the dimethyl ester, fractional distillation, and hydrolysis, as follows:

A solution of 5432 grams (20.4 mole) of the crude 3-(3-methoxybenzyl) adipic acid, 3410 grams (106.6 mole) methanol, 10.6 liters ethylenedichloride and 106 ml. concentrated sulfuric acid is stirred and refluxed for 15 hours. The mixture is cooled and washed with water (3X5 1.), 5 percent aqueous sodium hydroxide (1X2 1.) and again with water (3X5 1.). The ethylenedichloride solution is dried over 3 lb. anhydrous magnesium sulfate 19 (with 2' lb. Darco G60 activated carbon). The drying agent and carbon are filtered off and the filtrate concentrated at reduced pressure to remove solvent. The residue is distilled through a 3" x 16" vacuum-jacketed fractionating column packed with porcelain saddles. After a forerun of 934.1 grams, the product is collected at 172.0 C./0.2 mm. to 183 C./0.35 mm. This amounts to 3076.6 g. of 95 percent pure ester The ester, 2943.4 grams (10.00 mole) is hydrolyzed by heating over a steam bath for 19 hours with 1 kg. (25.0 mole) sodium hydroxide in 6 liters of water. The hydrolysis mixture is acidified to pH ca. 1.0 by addition of concentrated hydrochloric acid and the product is extracted-into methylene chloride (1x4 1. and 2x2 1.). The methylene chloride extract is Washed with water (1 X4 1. +1 8 1.), dried over magnesium sulfate, filtered and freed of solvent by distillation at reduced pressure. This gives 2506 grams of 3-(3-methoxybenzyl)adipic acid in the form of a very sticky oil.

Method C.A solution of dimethyl 3-(3-methoxybenzyl)adipate (0.01 mole) in 280 ml. of 1:1 tetrahydrofuran:1,2-dimethoxyethane at a temperature of about 10 C. is treated with a solution of sodium borohydride (0.005 mole) in 30 ml. of 1,2-dimethoxythane and ml. of water. After minutes, 5 ml. of glacial acetic acid is added and the mixture stirred for 5 minutes. Hydrocloric acid (3 ml. of 6 N) is then added, the mixture stirred for an additional 0.5 hour, then poured into water. The product, 3-[a-hydroxy-(B-methoxybenzyl)] adipic acid dimethyl ester, is recovered by evaporation.

The hydroxy ester is placed in 150 ml. of anhydrous hydrogen fluoride and allowed to stand overnight. The hydrogen fluoride is then evaporated and the thus produced dimethyl 3-(3-rnethoxy benzylidene)adipate dissolved in dioxane (300 ml.), treated with 0.3 g. of palladium on charcoal (5%) and subjected to 50 p.s.i. at room temperature until an equimolar proportion of hydrogen is consumed. The mixture is filtered and the filtrate evaporated to dryness under reduced pressure to give the desired compound as the methyl ester. It is hydrolyzed to the acid by the procedure of Method B.

EXAMPLE III Dimethyl 3-(2-chloro-5-methovybenzyl)adipate Method A.A mixture of 3.2 g. of dimethyl 3-(3- methoxybenzyl)adipate and 1.4 g. of N-chlorosuccinimide in 30 ml. of trifluoracetic acid is stirred and heated on a steam bath for 30 minutes. The reaction mixture is then poured into 5% aqueous sodium bicarbonate With stirring, and the mixture extracted with ether. The combined extracts are dried over anhydrous sodium sulfate and then concentrated under reduced pressure to an oil which is vacuum-distilled to obtain the product, B.P. 200 C. (1.1 mm. Hg).

Method B.A mixture of 3.2 g. of dimethyl 3-(3- methoxybenzyDadipate and 2.1 g. of phosphorus pentachloride in 100 ml. of dry benzene is refluxed for 30 minutes. The reaction mixture is carefully poured into ice and water, the benzene layer separated, washed with water and dried. Concentration of the dried benzene solution under reduced pressure yields an oil which is vacuum-distilled to obtain the product.

Similarly, the diethyl, dibenzyl and dipropyl chloroesters are prepared.

Method C.-A solution of 1688 g. of 3-(3-methoxybenzyl)adipic acid and 50 mg. of iodine in 9 liters of glacial acetic acid is stirred while a solution of 450 g. of chlorine in 8 liters of glacial acetic acid is added during about '2 hours. The mixture is kept in the dark during the procedure and the temperature maintained at 1015. C. The solvent is then removed by concentration under reduced pressure to give 1902 g. of a dark amber oil.

This procedure is repeated with ferric chloride in lieu of iodine with comparable results.

Method D.A mixture of 30.4 of diethyl 3-(3-methoxybenzyl)adipate and 12.75 g. of sulfuryl chloride in 250 ml. of benzene is allowed to stand for 3 days at room temperature. At the end of this period, the reaction mixture is concentrated under reduced pressure to a gummy residue which is vacuum-distilled to obtain the product.

Method E.The procedure of Method B is repeated using as starting compound the corresponding dicariboxylic acid to obtain 3-(2-chloro 5 methoxybenzyl) adipic acid dichloride.

EXAMPLE IV Diethyl 3-(2-chloro-S-ethoxybenzyl)adipate This product is obtained by the procedure of Method A of Example III employing diethyl 3-(3-ethoxybenzyl) adipate in lieu of dimethyl 3-(3-methoxybenzyl)adipate.

EXAMPLE V 2- 2-carbethoxyethyl) -5-methoxy-8-chloro-4tetralone Method A.A mixture of 2 g. of diethyl-3-(2-chloro- 5-methoxybenzyl)adipate (Example III) and 30 g. of polyphosphoric acid is heated on a steam bath for 30 minutes and then poured into ice Water. The oil then separates and is collected.

Method B.A mixture of 2.0 g. of the di-acid chloride of 3-(2-chloro-5-methoxybenzyl)adipic acid in 3 0 ml. of carbon disulfide is cooled to 0 C. and 4 g. of aluminum chloride added portionwise to the cooled mixture. The mixture is stirred for 30 minutes and then allowed to Warm to room temperature where a vigorous reaction ensures. After the vigorous reaction subsides the mixture is warmed on a steam bath, cooled, diluted with water and the carbon disulfide steam distilled. The mixture is extracted with chloroform and the product obtained by drying and concentrating the chloroform extract. The product is the free acid which, if desired, is converted to the desired lower alkyl ester by conventional methods. For example, the methyl ester is prepared as follows:

A mixture of 2002 g. (7.1 moles) of the tetralone acid, 3 l. chloroform, 682 g. (21.3 mole) methanol and 21.2 ml. conc. sulfuric acid is refluxed with stirring on a steam bath for 20 hours. The reaction mixture is then chilled and 2 1. each of chloroform and Water are added. The organic phase is separated and washed successively with two X2 1. water, one X1 1. 2% aqueous sodium hydroxide and three X 4 1. water to a final pH of about 7.5. After drying over anhydrous sodium sulfate and treatment with Darco KB activated carbon the solution is filtered and concentrated to a dark oil at reduced pressure. The oil is taken up in 6. 1. hot ethyl acetate and 11 l. hexane added. The solution is chilled to 5 C. with stirring and 1404 g. 2-(2-carbomethoxyethyl)-5- methoxy-S-chloro-4-tetralone recovered by filtration, hexane-washing and air-drying. The product melts at 101.0- 102.4 C.

EXAMPLE VI 2- 2-carboxyethyl -5-methoxy-8-chloro-4-tetralone A polyethylene container is charged with 1809 g. (6.03 mole) 3-(2-chloro-S-methoxybenzyl)adipic acid and chilled in an ice bath while 7 kg. liquid hydrogen fluoride is introduced from an inverted, chilled tank. The mixture is swirled to make homogeneous and then left to evaporate partially overnight in a hood. Most of the hydrogen fluoride that remains is removed by placing the polyethylene container in warm water to cause rapid evaporation. The remainder is removed by quenching in about 10 1. Water. The product is then extracted into chloroform, washed with water and dried over magnesium sulfate. Removal of the drying agent by filtration and the solvent by distillation gives a gum that is triturated with ether and filtered. This gives 1031 g. of crude product that is recrystallized from a mixture of 16 1. ethanol, 2 l. acetone and 1 l. ethylene dichloride, with activated carbon treatment. The first two crops amount to 863.9 grams of white crystalline product melting at 175.0- 180.5 C.

Elemental analysis gives the following results:

Calcd. for C H O Cl (percent): C, 59.47; H, 5.35; Cl, 12.54. Found (percent): C, 59.51; H, 5.42; Cl, 12.60.

Ultraviolet absorption shows x max at 223 m (s=24,650), 255 m (e=7,900) and 326 m (e=4,510). Infrared absorption maxima appear at 5.76 and 5.99 ,u.

This product is also obtained by hydrolysis of the product of Method A, Example V, by treatment with HCl in acetic acid.

The methyl ester, ethyl ester (m. 57-59 C.) and benzyl ester (m. 8485 C.) are prepared by conventional methods.

3-(3-methoxybenzyl)adipic acid, treated with. HF as described, yields 2 (2 carboxyethyl) 7 methoxy-4- tetralone, which melts at 1589 C. after two recrystallizations from benzene-hexane and exhibits ultraviolet absorption maxima at 225 m (e=13,500) and 276 m (e=16,000) in methanolic HCl and NaOH.

Analysis.-Calcd. for C H O (percent): C, 67.73; H, 6.50. Found (percent): C, 67.67; H, 6.48.

EXAMPLE VII 2- 2-carboxyethyl -6-chloro-7-methoxy-4-tetralone This substance is a byproduct of the cyclization of the products of Example III. It is separated from the crude 2-(2-carboxyethyl)-5-methoxy-8-chloro-4-tetralone of Example VI by virtue of its chloroform insolubility. 2900 g. of the crude tetralone are leached six times with 8 liter portions of hot chloroform. 170 g. of white solid remain, melting at 236239 C. The methyl ester is prepared by the procedure of Example V, Method B.

EXAMPLE VIII 2-(2-carbomethoxyethyl)-5-benzyloxy-8-chloro-4- tetralone 2 (2 carboxyethyl) 5 methoxy 8 chloro 4- tetralone g.), glacial acetic acid (200 ml.) and 48% hydrobromic acid (50 ml.) are heated at 90 under nitrogen for twenty-four hours. The cooled solution deposits a crystalline solid. The mixture is poured over two parts ice and the total solid crop isolated by filtration and thoroughly washed with water. The crude 2-(2-carboxyethyl)- 5-hydroxy-8-chloro-4-tetralone obtained in this way is recrystallized from acetonitrile to obtain 18.8 g. melting at 1648 C. elemental analysis.

Calcd. for C H ClO (percent): C, 58.11; H, 4.88; Cl, 13.20. Found (percent): C, 57.99; H, 4.87; Cl, 12.73.

14.5 g. of this product is placed in 200 ml. dry methanol and the mixture refluxed for minutes as anhydrous HCl is passed through. The now clear yellow solution is allowed to stand overnight, and the methanol is then removed in vacuo. The residual gum is extracted exhaustively with hexane and the combined extracts are concentrated and cooled. 11.8 g. of the white, crystalline methyl ester separates and is filtered off and recrystallized from hexane. The ester melts at 6869.5 C. and analyzes as follows:

Calcd. for C H CIO (percent): C, 59.45; H, 5.35, Cl, 12.6. Found (percent): C, 59.16; H, 5.38; CI, 12.6.

5.6 g. (0.02 mole) of this substance is dissolved in 500 ml. anhydrous methanol and to this is added 0.02 mole sodium methoxide and 500 ml. benzene. The mixture is concentrated to dryness in vacuo at room temperature, then heated at 100 C. and 0.1 mm. for 10 minutes. The residue is maintained under high vacuum at room temperature for 16 hours, and the dry solid added to 50 ml. benzyl bromide together with suflicient demethyl formamide to solubilize. The mixture is heated at 100 C. for

48 hours with stirring, then cooled and filtered. The filtrate is concentrated at reduced pressure and the residual oil chromatographed on acetone-washed and dried silicic acid in chloroform. The first effluent fraction consists of unchanged starting material. The main fraction, recognized by a negative ferric chloride test, deposits crystalline 2 (2 carbomethoxy ethyl) 5-benzyloxy-8-chloro-4- tetralone on standing.

EXAMPLE IX 2-carbomethoxy-5-methoxy-8-chloro-3,4,10-trioxo- 1,2,3,4,4a,9,9a,10-octahydroanthracene 30 grams of 2-(2-carbomethoxyethyl)-5-methoxy-8- chloro-4-tetralone (0.1 mole), prepared as described in Example V, Method B, is dissolved together with 24 grams dimethyloxalate (0.2 mole) by warming with 135 ml. freshly distilled dimethyl formamide in a well dried two'liter flask which has been flushed with dry nitrogen. The solution is cooled to 20 C. and to it is added all at onetime 0.4 mole sodium hydride in the form of a 50% oil dispersion which has been exposed to the atmosphere for 24 hours in order to produce a deactivating coating. The reaction mixture is maintained at 2025 C. with an ice bath. 0.1 mole dry methanol is now added, and the temperature rises spontaneously to 4050 C. When the temperature begins to fall (about 5 minutes after addition of the methanol) the reaction vessel is removed from the ice bath and quickly placed in an oil bath at 110 C. The reaction temperature is brought with dispatch to C. and maintained there for 10 minutes or until active bubbling ceases if this occurs sooner.

The flask is now immediately transferred back to the ice bath, and when the temperature reaches 15 C., ml. of glacial acetic acid is added at such a rate that the temperature does not exceed 30 C. At this point, a golden yellow precipitate appears. ml. methanol and 50 ml. water are added and the mixture is digested at 45 C. for 15 minutes and then stirred in an ice bath for an hour. If only a scanty crop of crystals is present at this time the mixture may be stored in the refrigerator overnight before processing. It is now transferred to a separatory funnel to permit separation of the oil from the sodium hydride oil dispersion. The suspension is then filtered with suction, and the filter cake triturated three times with 100 ml. portions of hot hexane to extract impurities. The washed solid is next stirred with 200 ml. water, filtered, and then digested with 500 ml. refluxing methanol for 20 minutes, to effect further purification. 15-16 grams of bright yellow needles are obtained. The product melts at 200-205 C. and exhibits no carbonyl absorption below 6 In 0.01 N methanolic HCl it exhibits ultraviolet absorption maxima at 406 mp (e=14,200) and at 275290 m (e=5,940). In 0.01 N methanolic NaOH it exhibits maxima at 423 my. (e=l3,950) and at 340 m (e=7,120).

EXAMPLE X 2-carbornethoxy-6-chloro-7-methoxy-3,4,10-trioxo- 1,2,3,4,4a,9,9a,10-octahydroanthracene 2 (2 carbomethoxyethyl) 6 chloro 7 methoxy- 4-tetralone, prepared in Example VII, 30 g., is dissolved in 24 g. dimethyl oxalate in 300 ml. dry distilled dimethyl formamide by warming. The solution is then cooled under nitrogen in an ice-salt bath and 19.86 g. sodium hydride (51.2% in oil) added all at once as the temperature is maintained below 20 C. The ice bath is removed and the temperature rises spontaneously to 30 C., whereupon the bath is replaced briefly to control the vigorous reaction. The reaction mixture is then heated to 70-80 C. for 5-8 minutes, cooled to below 0 C., and treated with 100 ml. acetic acid, added at such rate that the temperature does not reach 25 C. The reaction mixture is now poured into four volumes of chloroform. The chloroform solution is washed with Water, then with saturated brine, and dried over anhydrous sodium sulfate. The solvent is removed in vacuo, and the residue is treated with 350 m1. methanol. After standing for several hours at room temperature the slurry is filtered to obtain 12.5 g. yellow crystalline product, melting at 228231 C. with decomposition and gas evolution. Recrystallization from chloroform-methanol raises the melting point to 235.6-236.8 C.

Analysis.-Calcd. for (percent): C1qH15O5c1: C, 58.21; H, 4.31; Cl, 10.11. Found (percent): C, 58.53; H, 4.43; Cl, 10.10.

EXAMPLE XI 2-carb0benzyloxy-S-methoxy-S-chloro-3,4,l0-trioxo- 1,2,3 ,4,4a,9,9al-octahydroanthracene Z-(Z-carboxyethyl) --methoxy-8-chloro-4-tetralone, 0.02 mole, is combined with 500 ml. anhydrous methanol and to this is added 0.02 mole sodium methoxide and 500 ml. benzene. The mixture is concentrated to dryness in vacuo at room temperature, then heated at 100 C. and 0.1 mm. for minutes. The residue is maintained under high vacuum at room temperature for 16 hours, and the dry solid added to 50 ml. benzyl bromide together with sulficient dimethyl formamide to solubilize. The mixture is heated at 100 C. for 48 hours with stirring, then cooled and filtered. The filtrate is concentrated under reduced pressure to obtain the benzyl ester as residue. Purification is effected by washing of a chlorofohm solution With aqueous sodium bicarbonate.

This substance is dissolved together with 0.04 mole dibenzyl oxalate in 50 ml. dry, distilled dimethyl formamide. To this is added 0.08 mole sodium hydride in the form of a 50% oil dispersion, while maintaining the temperature at about -25 C. Benzyl alcohol, 0.02 mole, is added, and the mixture is heated to 80 C. for 5 minutes.

en cooled to 20 C. and slowly acidified with glacial acetate acid. The reaction mixture is next evaporated to -dryness under reduced pressure and the residue is taken up in chloroform. The chloroform solution is washed with water, then with brine, dried over sodium sulfate, treated with activated carbon and filtered. The filtrate is evaporated at reduced pressure to obtain the product as residue. It is purified by evaporation of the highly fluorescent, less polar eluate fraction from silicic acid chromatography in chloroform.

EXAMPLE XII 2-carbomethoxy-5-methoxy-8-chloro-3,4, lO-trioxo- 1,2,3 ,4,4a,9,9a10-octahydroanthracene Clean sodium metal (3.68 g.) is dissolved in methanol (50 ml.) and the solution evaporated to a dry white solid in vacuo (this is most successfully carried out by using rotary vacuum equipment). Dimethyloxalate (9.44 g.) and benzene (100 ml.) are then added to the flask and refluxing is carried out for about 10 minutes under nitrogen (not all of the solids dissolve but the cake is broken up). The solution is cooled and dimethylformamide (50 ml.) then added followed by the dropwise addition of a solution of 2-(2-car'boxyethyl)-5-methoxy-8-chloro-4-tet ralone (Example VI) (11.3 g.) in dimethylformamide (100 ml.) during one hour at 20 under N with stirring, and stirring at room temperature under N is continued overnight. The solution is then poured into cold water (1 l.) and extracted twice with chloroform. The chloroform extract is discarded and the aqueous solution acidified with 10% HCl solution. The product is obtained by extraction with chloroform (3 X200 ml.), backwashing once with water, drying over anhydrous Na SO treatrnent with charcoal, filtration and evaporation of the solvent in vacuo to give a red gum (16.4 g.) which is 2-(2- carboxyethyl) 3 methyloxalyl 5 methoxy-9-chloro-4- tetralone.

U.V. absorption maxima in 0.01 N NaOH at 258 and 363 the. maximum in 0.01 N HCl at 347 mu, minimum at 277 mu.

The gum gives a deep red color with ferric chloride in methanol and liberates CO from a saturated NaHCO solution.

The acid is esterified by dissolving in chloroform (1 1.), methanol (50 ml.) and cone. H 50 (10 ml.) and refluxing gently for 15 hours. The solution is cooled, poured into excess water and the chloroform layer separated. The aqueous layer is extracted with chloroform (250 m1.) and the combined chloroform extracts are backwashed twice with cold water. The extract is then dried over anhydrous sodium sulphate, treated with activated charcoal, filtered and evaporated to a red gum in vacuo. This gum does not liberate CO from saturated bicarbonate solution, and gives a deep red color with ferric chloride in methanol.

The ester product, 3.825 grams, and 1.275 g. of sodium hydride (56.5% solution in oil) are dissolved in 25 ml. of dimethylformamide. An exothermic reaction sets in with the evolution of hydrogen gas. After the evolution of gas ceases the mixture is warmed at C. for /2 hour where further evolution of hydrogen gas occurs and the reaction mixture darkens. The reaction mixture is finally digested on a steam bath for 10 minutes after which it is cooled and acidified with glacial acetic acid (15 ml.). The product is then obtained by dilution of the mixture with water followed by extraction with chloroform. The dried chloroform solution is concentrated under reduced pres sure to obtain a gummy residue which crystallizes on trituration in methanol. The orange-yellow crystalline product, 2 carbomethoxy 5 methoxy-8-chloro-3,4,10-trioxo- 1,2,3,4,4a,9,9a,lO-octahydroanthracene, (1.2 g.) melts at 196-20l.5 C.

EXAMPLE XIII Z-carbomethoxy-S-hydroxy-8'-chloro-3,4,10-trioxo- 1,2,3,4,4a,9,9al0-octahydroanthracene Dimethyl oxalate, 0.84 g., and 2-(2-carbomethoxyethyl)-5-hydroxy-8-chloro-4-tetralone, 2.0 g., are added to a suspension of 0.34 g. sodium hydride in 10 ml. dimethyl formamide and the mixture is heated to 70 C. for three minutes. After cooling, the reaction mixture is treated with 10 ml. acetic acid and evaporated to dryness at reduced pressure. The residual gum is triturated with water to remove sodium acetate and chromatographed on silicic acid in chloroform. The main efiiuent fraction is dried to a bright yellow solid which is crystallized from chloroform-hexane to provide 380 mg. product melting at 218- 219.5 C. Elemental analysis, calculated for C H O Cl (percent): C, 56.7; H, 3.9; CI, 10.5. Found (percent): C, 56.86; H, 3.89; Cl, 10.8.

EXAMPLE XIV Diethyl 3-(u-hydroxy-B-methoxybenzyl)adipate This product is obtained by treating 5 g. diethyl 3-(3- methoxybenzoyl)adipate and 2 g. 5% palladium on carbon in ethanol with 40 p.s.i. hydrogen gas at room temperature until one molar equivalent of hydrogen is consumed. The reaction mixture is filtered and concentrated at reduced pressure to obtain the product.

It is further converted to diethyl 3-(a-N,N-dimethylamino-S-methoxybenzyl in the following manner:

The m-hydroxy benzyl adipate ester, 0.01 mole in 15 ml. dimethoxyethane, is added to a stirred mixture of 1.9 g. (0.01 mole) p-toluenesulfonyl chloride and 2.5 ml. dry pyridine in an ice bath. When the reaction subsides the mixture is permitted to warm to room temperature, stirred for three hours, and poured into ml. water. The pH is adjusted to 5 and the resulting tosyl ested recovered by filtration.

The tosylate (0.0025 mole) is combined with 25 ml. dirnethoxyethane and added dropwise to a stirred solution of 0.015 mole dimethylamine in 50 ml. dimethoxyethane at 0 C. After addition is complete, stirring is continued for an hour at 0 and the reaction mixture is then heated at for three hours under a Dry Ice condenser. The mixture is next evaporated in vacuo and the residue washed with water to remove dimethylammonium toluenesulfonate. The product is recovered by filtration from the water. Substitution of monomethylamine for dimethyl-.

amine in this procedure provides the corresponding a-N- methylamino derivative.

EXAMPLE XV 2-(2-carbomethoxyethyl) -5-methoxy-4-tetralone 2 (Z-carbomethoxyethyl)-5-methoxy-8-chloro-4-tetralone (1.5 g.) is combined with 5% palladium-on-charcoal (0.37 g.), triethylamine (0.5 g.) and methanol 270 ml. in a standard Parr hydrogenation bottle and subjected to 50 pounds of hydrogen pressure. The absorption of hydrogen levels off at approximately one molar equivalent. The catalyst is filtered off, the solution taken to dryness, and triethylamine hydrochloride is removed by washing with water. The residual white solids weigh 1.1 g. and melt at 6366 C. After two recrystallizations from hexane and one from ether and product melts at 85-87 C.

Analysis.--Calcd. for C H O (percent): C, 68.68; H, 6.92. Found (percent): C, 68.59; H, 6.98.

EXAMPLE XVI 2-(2-carboxyethyl)-7-hydroxy-4-tetralone 3-(3-methoxybenzyl)adipic acid, 22.46 g., is heated at reflux with hydriodic acid (specific gravity 1.5) for 3 hours and the methyl iodide formed is separated. The solution is evaporated in vacuo and the resulting gum triturated with cold water to yield 14.7 g. of yellow crystalline product. Dried and recrystallized from aqueous acetone the product is obtained in the form of white crystals melting at l83.5l85.5 C. Elemental analysis, calculated for C H O (percent): C, 66.65; H, 6.02. Found (percent): C, 66.60; H, 6.02.

The same product is obtained by refluxing a mixture of 0.5 g. of the 3-(3-methoxybenzyl)adipic acid with 25 ml. 48% HBr for 18 hours, then pouring the reaction mixture into 3 volumes of Water, and filtering the resulting 0.4 g. of crystalline precipiate.

EXAMPLE XVII 2- 2-carbomethoxyethyl) -S-methoxy-S-nitro-4-tetralone One gram of the Example XV product is slowly added to ml. of concentrated sulfuric acid containing 2 ml. of 70% nitric acid at a temperature of O-5 C. The solution is stirred for minutes and allowed to warm to room temperature. The mixture is poured into icewater mixture and extracted with chloroform, the chloroform layer separated, dried and concentrated to obtain the product.

EXAMPLE XVIII 2-(2-carboxyethyl)-5-hydroxy-8-amino-4-tetralone One molecular proportion of aniline is dissolved in 2 N HCl, employing about 20 ml. thereof per gram of aniline, and the solution treated with one molecular proportion of NaNO at 0 to 10 C. The benzenediazonium chloride solution is then mixed with stirring at 0 to 20 C. with an aqueous solution of 2-(2-carboxyethyl)-5-hydroxy-4-tetralone sodium salt and sufiicient sodium carbonate to neutralize the excess HCl in the diazotised aniline solution. The pH of the solution is in the range 810. Stirring is continued at 0 C. for approximately two hours after which careful neutralization of the reaction mixture yields the 8-phenylazo compound. The product is collected on a filter, washed and dried.

One part by weight of 2-(2-carboxyethyl)-5-hydroxy-8- phenylazo-4-tetralone is mixed with 20 parts by weight of methanol and part by weight of 5% palladium-on carbon catalyst is added to the mixture which is then hydrogenated at -45 p.s.i. of hydrogen gas in a conventional shaker apparatus at 30 C. until two molar equivalents of hydrogen are taken up.

After filtration, the product is recovered by high vacuum distillation of the residue obtained by removal of the solvent in vacuo. Care must be exercised to protect the amino phenol from air. It can be stabilized by acetylation, as follows:

The crude amine is placed in 20 parts water containing one molar equivalent of HCl, and 2.2 molar equivalents of acetic anhydride are added. Suflicient sodium acetate is then added to neutralize the HCl and the solution is warmed to 50 C. After 5 minutes the mixture is cooled and the crude acetate separated by filtration. The solid is then dissolved in cold 5% sodium carbonate solution and reprecipiated with 5% HCl. The 2-(2-carboxyethyl)- 5-hydroxy-8-N-acetylamino-4-tetralone obtained in this manner is a preferred form of the amino compound for further reaction sequences.

EXAMPLE XIX 3-(2-amino-5-hydroxybenzyl)adipic acid The procedure of Example XVIH is repeated using 3- (3-hydroxybenzyl)adipic acid as starting compound to obtain this product. It may be converted to the product of Example XVIII by the ring closure procedure of Example VI.

EXAMPLE XX 3-(2-chloro-5-hydroxybenzyl)adipic acid Three parts by weight of the product of Example XIX (obtained by evaporating the methanol) is protected from air, immediately mixed with 10 parts by weight of 10% aqueous hydrochloric acid at 0 C., and diazotized by gradual addition of 20% aqueous sodium nitrile solution. Addition of sodium nitrite is continued until a positive starch iodide test on a few drops of the reaction mixture is obtained in the conventional fashion. The resulting so lution is then added to 15 parts of a boiling 10% solution of cuprous chloride in aqueous hydrochloric acid. The mixture is boiled for 10 minutes and allowed to cool. The product separates from the cooled mixture and is collected in the conventional manner.

This procedure is used for the preparation of 3-(2-substituted-S-hydroxy-benzyl)adipic acid compounds such as 2-bromo (using Cu Br and HBr), 2-iodo (using KI and H EXAMPLE XXI 3 [a-hydroxy-u- (2-chloro-5-methoxy-phenyl) ethyl] adipic acid diethyl ester EXAMPLE XXII 3-[a- 2-chloro-5-methoxyphenyl)ethyl]adipic acid diethyl ester The product of Example XXI, 2 g., is dissolved in ml. of glacial acetic acid and hydrogenated at a pressure of 40 p.s.i. of hydrogen gas for 24 hours at room temperature in the presence of 2 g. of 5% palladium-in-carbon catalyst. The mixture is filtered and then concentrated. The product is obtained by vacuum distillation of the residue.

EXAMPLE XXIII 3,3,4-trimethoxybenzophenone A mixture of 40 g. of 3-rnethoxybenzoyl chloride, 32 g. of veratrole and 250 m1. of carbon disulfide in a 3 neck round bottom flask fitted with reflux and stirrer is cooled to 0 C. Then 40 g. of aluminum chloride is added portionwise to the cooled mixture and the mixture stirred for 45 minutes, after which it is allowed to warm to room temperature. A vigorous reaction ensues with the separation of a yellow precipitate. The mixture is carefully warmed on a steam bath and stirred for 1 /2 hours. Water is then added to the cooled mixture and the carbon disulfide is steam distilled off. The resultant mixture is then extracted with chloroform and the chloroform layer separated, washed with dilute hydrochloric acid, followed by dilute sodium hydroxide and then dried and concentrated under reduced pressure. The residual oil is distilled to obtain the product, B.P. 2l6218 C. at 1.5 mm. mercury. A 65% yield of product is obtained. The viscous product is stirred in absolute methanol and crystallizes, In. 8586 C.

EXAMPLE XXIV 3 ,3',4-trirnethoxydiphenylmethane Method A.A solution of 5 g. of 3,3,4-trimethoxybenzophenone in 200 ml. of ethanol containing 1 g. of copper chromium oxide is hydrogenated at 180 C. and 100 atmospheres of hydrogen gas for 1.5 hours. The resultant solution is filtered and concentrated under re duced pressure. The residual oil is distilled to obtain the product B.P. 192194 C. at 2.5 mm. mercury. The product crystallizes on standing, the melting point of the crystals being 4546 C. Elemental analysis gives the following results:

Calcd. for C H O (percent): C, 74.39; H, 7.02. Found (percent): C, 74.50; H, 7.18.

Method B.This product is also obtained by hydrogenation of the starting compound of Method A using 10% palladium on carbon in ethanol at 50 C. and 40 psi. of hydrogen gas. The hydrogenation procedure is also carried out at room temperature, although the uptake of hydrogen is considerably slower than at 50 C. The product is obtained by filtration and concentration of the hydrogenation mixture.

EXAMPLE XXV 3,3,4-trihydroxydiphenylmethane Two grams of 3,3,4-trimethoxydiphenylrnethane are dissolved in 10 ml. of acetic acid and 10 ml. of 48% hydrobromic acid and the mixture refluxed for 5 hours. The reaction mixture is concentrated under reduced pressure to obtain a residual gum which is vacuum-distilled (B.P. 230 C. at 0.5 mm. of mercury). The distillate, a colorless gum, crystallizes. .A 62% yield of product is obtained, In. 103.5-104 C.

EXAMPLE XXVI 3-(3-hydroxybenzy1)-hexa-2-4-di-enedioic acid A mixture of 3.5 g. of 3,3',4-trihydroxydiphenylmethane in 50 m1. of acetone and 50 ml. of 10% aqueous sodium hydroxide is cooled to C. Thirty ml. of 35% aqueous hydrogen peroxide solution is then added dropwise, the mixture turning pale pink after to minutes. An exothermic reaction occurs with considerable boiling and foaming. The mixture is allowed to stand for 1 hour and is then extracted with ethyl acetate, the extract being dicarded. The aqueous solution is then acidified and extracted with ethyl acetate. Concentration of the ethanol acetate extract after drying gives the product as a gummy residue.

EXAMPLE XXVII 3-(3-hydrdxybenzyl)adipic acid The product of the preceding example (105 mg.) is dissolved in 13 ml. of ethanol containing 1 drop of concentrated hydrochloric acid and hydrogenated over platinurn oxide at 1 atmosphere of hydrogen gas at room temperature. The hydrogen uptake is exactly 2 molecular equivalents. Filtration and concentration of reaction mixture gives the product.

2B EXAMPLE XXVIII 3-(3-methoxybenzyl)adipic acid dimethyl ester The acid product of the preceding example is dissolved in aqueous sodium hydroxide (4 molar equivalents) and agitated with 3 molar equivalents of dimethyl sulfate at 40 C. for 6 hours. The resultant solution is then diluted with water and extracted with chloroform. The chloroform layer is separated, dried and concentrated under reduced pressure to yield an oil, B.P. 205 to 210 C. at 0.2 mm. mercury. This product is also obtained by treatment of the starting compound with diazomethane in diethyl ether.

In a similar manner the corresponding ethyl and propyl esters are prepared.

EXAMPLE XXIX 3- (3-methoxybenzyl)hexa2,4-dienedioic acid Five grams of 3,3',4trimethoxydiphenylmethane are dissolved in 50 ml. of acetic acid containing about 10 drops of water and ozonized air containing about 4% O is then passed into the mixture for 1.5 hours (total of about 6 moles of ozone). The resultant yellow solution is poured into 1 liter of water and extracted with chloroform. The chloroform layer is separated, washed with aqueous sodium bicarbonate solution and concentrated under reduced pressure. The residue is dissolved in ethanol containing 2 g. of KOH and the mixture allowed to stand at room temperature for 2 days after which it is diluted with water and extracted with chloroform. After separation of the chloroform layer the aqueous alkaline solution is acidified with dilute hydrochloric acid and extracted with chloroform. Concentration of the chloroform extract gives the acid product.

The methyl, ethyl and propyl diesters of this acid are prepared by refluxing the acid for 3 days in ethylene dichloride containing the appropriate alcohol and sulfuric acid.

EXAMPLE XXX 3-(3-rnethoxybenzyl)adipic acid dimethyl ester The ester of the preceding example is hydrogenated in ethanol over 10% palladium on carbon at 1 atmosphere of hydrogen gas at room temperature. The theoretical uptake of hydrogen gas (2 molar equivalents) is very rapid. The product is obtained by filtration and concentration of the hydrogenation mixture.

In similar fashion the corresponding free acid is obtained by hydrogenation of the free acid of the preceding example.

EXAMPLE XXXI The following monoester compounds are prepared by reduction of corresponding benzoyl diesters according to the methods of Example I. The free adipic acid derivatives are prepared by the methods of Example II from the corresponding benzoyl adipic acids. The products are subsequently converted to the corresponding diesters by conventional procedures, e.g., Example II, Method B.

3-benzyladipic acid monoethyl ester 3-(Z-ethyl-S-hydroxybenzyl)adipic acid monoethyl ester 3-(2-chloro-5-methoxybenzyl)adipic acid monomethyl ester 3-(2-dimethylamino-S-methoxybenzyl)adipic acid monomethyl ester 3- Z-amino-S-methoxybenzyl) adipic acid 3- (Z-acetamido-S-rnethoxybenzyl) adipic acid 3-(3-hydroxy-benzy1)adipic acid monoethyl ester 3-(3-methyl-5-hydroxybenzyl)adipic acid monoethyl ester 3-(2,3-dimethyl-5-hydroxybenzyl)adipic acid monoethyl ester 3-(Z-methyl-S-hydroxybenzyl) adipic acid monoethyl ester 3-(3-dimethylamino-S-hydroxybenzyl)adipic acid monoethyl ester 3-(2,3-dimethylbenzyl)adipic acid monomethyl ester 3-(3,5-dimethoxybenzyl)adipic acid monoethyl ester 3-(3-hydroxybenzyl)adipic acid monoethyl ester 3-(3-isopropyl-S-hydroxybenzyl)adipic acid monoethyl ester 3-(2,3-diethyl-5-hydroxybenzyl)adipic acid monoethyl ester 3-(5-benzyloxybenzyl)adipic acid monoethyl ester 3-(2-chloro-5-benzyloxybenzyl) adipic acid monoethyl ester 3-(3-propionyloxybenzyl)adipic acid monoethyl ester 3-(3-acetyloxybenzyl)adipic acid monoethyl ester 3-(2-amino-S-benzyloxybenzyl)adipic acid monobenzyl ester 3-(2-propyl-5-propoxybenzyl)adipic acid monomethyl ester 3- (S-methoxy-Z,3-ditrifluoromethylbenzyl) adipic acid monomethyl ester 3- 2-trifiuoromethyl-3,5-dibutoxybenzyl adipic acid monomethyl ester 3-(2-trifluoromethyl-3-ethylamino-S-methoxybenzyl) adipic acid monoethyl ester 3-(3 butyrylamidobenzyl)adipic acid monoethyl ester 3- 2-trifiuoromethyl-S-hydroxybenzyl) adipic acid monobenzyl ester 3-(2-chloro-5-hydroxybenzyl)adipic acid monobenzyl ester 3-(2-chloro-3-methyl-5-hydroxybenzyl)adipic acid monoethyl ester 3-(2-chloro-3-isopropyl-5-hydroxybenzyl)adipic acid monoethyl ester 3- (2-chloro-3-amino-5-methoxybenzyl) adipic acid monoethyl ester 3-(2-chloro-3-methyl-5-methoxybenzyl) adipic acid monobenzyl ester 3- 2-chloro-3-ethyl-5-methoxybenzyl adipic acid monobenzyl ester 3-(2-chloro-3-dimethylamino-5-hydroxybenzyl)adipic acid 3-(3,5-dimethoxybenzyl)adipic acid monoethyl ester 3-(Z-methylamino-5-propoxybenzyl)adipic acid monoethyl ester 3-(Z-methyl-S-hydroxybenzyl) adipic acid 3-(Z-amino-S-benzyloxybenzyl)adipic acid monomethyl ester 3-(3-acetamido-S-hydroxybenzyl)adipic acid monoethyl ester 3-(2-chloro-3,S-dihydroxybenzyl)adipic acid monoethyl ester 3-(3-trifiuoromethyl-S-hydroxybenzyl)adipic acid monoethyl ester 3-(3-hydroxybenzyl)adipic acid monoethyl ester The corresponding diesters are prepared by esterification of these compounds with the selected alcohol by the usual method.

Those compounds having a benzyloxy substituent are reduced by the procedures of Methods A or C of Example II. Of course, the procedure of Example II, Method A, results in hydroylsis of the ester groups and necessitates re-esterification.

EXAMPLE XXXII Alpha-hydroxybenzyladipic acid compounds corresponding to the products of Example XXXI are prepared by hydrogenation of corresponding benzoyladipic acid compounds according to the method of Example XIV.

The a-hydroxybenzyl adipate diesters are further converted to the corresponding a-dimethylamino and a-monomethylamino derivatives via the tosylates by the procedure described in Example XIV. For this procedure hydroxy substituents other than the a-hydroxy group are avoided by employing the corresponding methyl ethers;

likewise, amino substituents are employed in acetylated form.

The a-amino benzyl adipates obtained in this manner are further converted to the corresponding 1-amino-4- tetralones of structure III by the procedure of Example VI.

EXAMPLE XXXIII The procedure of Example XXI is repeated to produce the following compounds from corresponding benzoyladipic' acid compounds using lower al-kyl-magnesium halides.

diethyl 3- a-hydroxy-a-phenethyl) adipate diethyl 3-[a-hydroxy-ot-(Z-ethyl-S-hydroxyphenyl) ethyl]adipate dimethyl 3- a-hydroxy-u- Z-dimethylamino-S-methoxyphenyl ethyl] adipate dimethyl 3- a-hydroxy-u- Z-amino-S-methoxyphenyl) ethyl] adipate dimethyl 3-[u-hydroxy-a-(2-acetamido-5-methoxyphenyl ethyl] adipate diethyl 3- [et-hydroxy-ot- 3-hydroxyphenyl) ethyl] adipate diethyl 3-[a-hydroxy-u-(2-chloro-5-methoxyphenyl) ethyl] adipate diethyl 3- ot-hYdIOXY-a- (3 -methyl-5-hydroxyphenyl) ethyl]adipate diethyl 3-[a-hydroxy-a-(3,5-dimethoxyphenyl)ethyl] adipate diethyl 3- a-hydroxy-u- 3-methoxyphenyl) propyl] adipate diethyl 3-[a-hydroxy-a-(Z-chloro-S-methoxyphenyl) propyl]adipate diethyl 3- [a-hydroxy-m- 2-chloro-5-methoxyphenyl) butyl] adipate diethyl 3- oz-hYdIOXY-oc- 3-methoxyphenyl) ethyl] adipate In the case of the precursors to the compounds listed above which possess an active hydrogen, 2.5 moles of Grignard reagent are employed.

The compound-s containing an amino-substituent are isolated from the reaction mixture by the substitution of saturated aqueous ammonium chloride for 6 N HCl.

EXAMPLE XXXIV The a-hydroxy group of Example XXXIII compounds is hydrogenolyzed according to the method of Example XXII to afford the following compounds:

diethyl 3- (a-phenethyl) adipate diethyl 3- [a- 2-ethyl-5-hydroxyphenyl) ethyl] adipate dimethyl 3- a- 2-chloro-5-methoxyphenyl) ethyl] adipate dimethyl 3- [a- (Z-dimethylamino-S-methoxyphenyl) ethyl] adipate dimethyl 3- [Z-amino-S-methoxyphenyl ethyl] adipate dimethyl 3- [a- 2-acetamido-S-methoxyphenyl propyl] adipate diethyl 3- [a- 3-hydroxyphenyl) ethyl] adipate diethyl 3- a- 3-methyl-5-hydroxyphenyl ethyl] adipate diethyl 3- [oc- 3 ,5 -dimethoxyphenyl ethyl] adipate diethyl 3- [a-(3-methoxypheny1) propyl] adipate diethyl 3- [a-2-chloro-5-methoxyphenyl propyl] adipate diethyl 3- u- 2-chloro-5-methoxyphenyl) butyl] adipate diethyl 3- [w (3 -methoxyphenyl) ethyl] adipate EXAMPLE XXXV The following compounds are prepared according to the methods of Example VI by ring closure of corresponding compounds.

2- 2-carbethoxyethyl) -4-tetralone 2- 2-cyanoethyl 5 -methoxy-8-ethyl-4-tetralone 2- Z-carboxyethyl) S-methoxy-8-dimethylamino-4- tetralone X X; X: A A5 H H H H COOEt H S-Et 5-OMe H CN H B-NMeg 5-OMe H COOEt H S-NH: S-OBZ H COOMB H S-NHGOMe 5-OMe H C OOPr H H 5-OH H COOBZ 7-Me H 5-OH H CO E1; 7-i-Pl H -OH H COOBZ T-Et S-Et 5-OH H COOMB H H 5-0CH2C6H5 H COOBZ H H 5-OH H COOEI; 7-NH2 H 5-OM8 H COOBZ 7-P1' H 5-OM8 H COOBZ 7-DI8 H 5-OM8 H COOBZ 7-Nhleg H 5-OH H COOBZ 7-Me S-Me H H COOMG H S-NHg 5-OCH2C5H5 H COOMe H 8-Pl 50]?! H COOMe H H 5-OH H COOMB H H S-OIVIB M6 COOMB H H 5-OMe ET, OOOMe H H 5-0Me Pr COOMe H 8-l\Ie 5-OM8 H CN H (i-NIB 5-OH H COOBZ 7-Me S-NIG 5-0H H COOBZ H H 5-0H M8 COOBZ H H 5-OH i-PI COOBZ II H 5-OM8 M8 COOBZ H H 5-OhI8 H COOBZ H H 5-0NIB Et C O OBZ 7-CF 8-CF 5-OMe' H OOMG T-EtCOZ B-IVIG H EEOCH(MQ) COOEII 7-OBu 8-CF3 5-OBu H OOEt 'T-NHEI; 8-C F E-OIVIB H COOEt T-NHCOCaH'! H H H COOMe 7-MeC0z 8-01 5-OEt Et COOMe H 8-CF H H COOBZ H 8*Cl 5OH H COOBZ 7-BIG 8-Cl 5-OH H COOEt H B-NHMB 5-OPI H COOEt H S-CI 5-OBZ H COOBZ 7-1\I8 B-CI 5-OM8 H COOBZ 7-NH2 8-CI 5-OM9 H COOBZ 7-El. 8-Cl 5-0M6 H COOBZ H 8-C1 5-OMe Me COOMB H 8-Cl S-OIVIB El; COOMG II 8-Cl 5OH9 Pl COOMB 'Z-UDIG H S-OIVIB H COOEC H 8-Cl 5-0Me MeOCHz COOMe H 8-01 5-OH MGOCHQVIG) CO 0M8 7-Me 8-01 5-03: HO CH(C5H11) C O OMe H 8-01 H 1M6 OOEI; H 8-CF 5-OMI6 B19 COOEt H H 5-Oh/I8 MBOCHz COOEt 7-Et H 5-OMI8 H COOBZ 7-i-P1 8-01 5-OH .H CO OH H H 5-OEt M6 COOBZ 7-Nl\ Ieg 8-CI 5-OM8 H C O OBI]. 7-0116 8-0]. H COOBU 7-NHCOCH3 8-01 5-OMe H COOMG 7-NHCOCH H 5-OH H COOEI; 7-OH B-CI 5-OH H COOEt H 8-CF 5-OH H COOBZ 7-CF H 5-OH H COOEt 7-OB3 H M9 COOEI;

In the above table, Me=CH Et=C H P1'=C H Bz=benzyl. Ether substituents are converted to hydroxy groups by HBr cleavage; and acylamido groups to amino groups by hydrolysis.

EXAMPLE XXXVII 5-methoxy-8-chloro-3,4,l0-trioxo-1,2,3,4,4a,9,9a,l0- octahydroanthracene Method A.A mixture of 10 g. of the ester product of Example XII, 250 ml. of glacial acetic acid, 125 ml. conc. HCl and ml. of water is heated at 95 C. for 1 hour. During the first minutes considerable effervescence occurs and the suspended matter gradually dissolves to give a deep red-brown solution. The reaction mixture is then poured into 2 liters of cold water and extracted with chloroform. The combined extracts are washed with water, decolorized with activated carbon, dried and evaporated to an orange-crystalline solid (6.9 g.) which melts at l71-172.8 C. After recrystallization from acetonehexane, the product melts at 172173 C.

Method B.The 2-carbobenzyloxy compound (5 g.) corresponding to that of Example XII is treated with hydrogen gas at room temperature in acetic acid and in the presence of 0.5 g. of 5% palladium on carbon at 50 p.s.i.g. until one molar equivalent of gas is taken up. The product is obtained by filtration and concentration of the reaction mixture after warming to 60 C. for 20 minutes to ensure complete evolution of carbon dioxide.

Method C.The product of Example XII (3 g.) is refluxed for 3 hours in 10 ml. of acetic acid, 10 ml. of concentrated sulfuric acid and 1 m1. of water after which chloroform is added to the mixture which is then poured into excess water. The product is obtained by separation of the chloroform layer, washing, drying over sodium sulfate and concentration. A solid residue is obtained and recrystallized from methanol.

If desired, further purification is achieved by chromatography on silicic acid with chloroform elution.. The product is contained in the less polar effluent fraction.

EXAMPLE XXXVIII The products of Example XXXVI are decarboxylated (benzyl esters by hydrogenolysis according to Method B, Example XXXVII and lower alkyl esters and nitriles by the procedure of Method C, Example XXXVII) to EXAMPLE XLI t-butyl ester of (3-methoxybenzoyl)acetic acid To a stirred suspension of sodamide in liquid ammonia (prepared from 11.5 g. of sodium in 400 ml. of liquid ammonia) is added 54 g. of t-butyl acetate in 50 m1. of dry ether followed by a solution of 41.5 g. of methyl 3-methoxybenzoate in 50 ml. of dry ether. The ammonia is then replaced by 100 ml. of ether and the mixture refluxed for 2 hours. After standing at room temperature for 12 hours, the mixture is poured into 400 ml. of ice water containing 28.8 ml. of acetic acid. The mixture is then extracted with ether, the etherate washed with 2% sodium bicarbonate solution and then dried over anhydrous sodium sulfate. After removal of the ether at reduced pressure, the residual oil is distilled in vacuo to obtain 33.5 g. of product, B.P. 126-128 (0.3 mm.). Infrared absorption of the product shows characteristic maxima at 5.75 and 5.90.

EXAMPLE XLII Ethyl 3-carbomethoxy-3-(3-methoxybenzoyl)propionate Method A.To a suspension of 26 g. of sodium hydride in 250 ml. of dry dimethylformamide is added dropwise with stirring at room temperature a solution of 108 g. of the Example XL methyl ester in 250 ml. of dry dimethylformamide over a period of 45 minutes. The mixture is stirred for an additional 30 minutes and there is then added dropwise with stirring a solution of 104 g. of ethyl bromoacetate in 250 ml. of dry dimethylformamide. The mixture is allowed to stand for 12 hours and is then evaporated under reduced pressure. The residual oil is dissolved in chloroform and the solid sodium bromide filtered. The chloroform solution, after water-washing and drying over sodium sulfate, is evaporated and the residual oil distilled in vacuo to obtain 112.5 g. of product, B.P. 18.2-188 C. (1.4-1.5 mm.). Infrared analysis of the product shows characteristic peaks at 5.75 and 5.91 microns.

Elemental analysis gives the following results:

Calcd. for C H O (percent): C, 61.21; H, 6.17. Found (percent): C, 61.39; H, 6.23.

Ethyl and propyl 3-carbethoxy-3-(3-methoxybenzoyl) propionate are prepared in similar fashion.

Method B.To a mixture of 29 g. of methyl 3-methoxybenzoate and 15 g. of sodium hydride in 75 ml. of dry dimethylformamide is added a solution of 19 g. of dimethyl succinate in 175 ml. of the same solvent dropwise with stirring at room temperature during 12-14 hours. The mixture is carefully acidified with ml. of acetic acid and stirred at room temperature for an additional 3 hours. The filtered reaction mixture is next evaporated to a residue consisting of an oil and solid which is is treated with ether to dissolve the oil. The ether solution is filtered and evaporated under reduced pressure to yield 18.29 g. of dimethyl a-[3-methoxybenzoyl]succinate, B.P. 162.9 C. (04-05 mm.). Infrared analysis of the product shows characteristic peaks at 5.75 and 5.90 microns.

Elemental analysis gives the following results:

Calcd. for C H O (percent): C, 59.99; H, 5.75. Found (percent): C, 59.91; H, 5.79.

In similar manner, the corresponding diethyl, dipropyl and di-t-butyl esters are prepared.

EXAMPLE XLIII Ethyl 3-carbot-butoxy-3-(3-methoxybenzoyl)propionate A mixture of 15.8 g. of the product of Example XLI 10.5 g. of ethyl bromoacetate and 3.02 g. of sodium hydride in 130 ml. of dimethylformamide is treated as in Method A of Example XLII to obtain this product as a yellow oil. Infrared analysis of the product shows characteristic peaks at 5.75 and 5.90,u.. The product is used without distillation in the procedure of Example XLVI to produce ethyl 3-[carbo-t-butoxy-3-(2-cyanoethyl)-3- (3-methoxybenzoyl) ]-propionate.

EXAMPLE XLIV Diethyl 3-carbethoxy-3- 3-methoxybenzoyl adipate To a mixture of 102 g. of diethyl a-(3-methoxybenzoyl)succinate in 250 ml. of dioxane and 10 ml. of a 35% solution of benzyltrimethylammonium hydroxide in methanol maintained at 50 C. is added 167 g. of ethyl acrylate in one portion with stirring. Heating and stirring are continued for 30 minutes, after which 10 ml. of glacial acetic acid is added. The mixture is evaporated under reduced pressure to a dark oil which is distilled in tilled in vacuo to yield 80.5 g. of the diethyl ester product, B.P. 197 C. (0.1-0.2 mm.), n =l.5043. Infrared analysis shows characteristics peaks at 5.76 and 5.92

Elemental analysis gives the following results:

Calcd. for C H O (percent): C, 61.75; H, 6.91. Found (percent): C, 61.64; H, 6.90.

Dimethyl and dipropyl ,B-carbomethoxy-3-(3-methoxybenzoyl)adipate are prepared in similar fashion.

EXAMPLE XLV Diethyl 3-carbo-t-butoxy-3-(3-methoxybenzoyl)adipate The product of Example XLIII a yellow oil, is dissolved in ml. of t-butanol containing 0.75 g. of potassium t-butoxide and 19 g. of ethyl acrylate. The mixture is refluxed for 1.3 hours and then concentrated under reduced pressure to obtain the adipate ester product, a yellow viscous oil, which is used without distillation in the procedure of Method B of Example XLVII.

EXAMPLE XLVI Ot-(3-II16tl'lOXYb6I1ZOYl) -a- (Z-cyanoethyl) succinic acid diethyl ester This compound is prepared according to the procedure of Example XLIV using acrylonitrile or B-bromopropionitrile in lieu of ethyl acrylate. The product is vacuum distilled at 212-218 C. (0.45 mm. Hg). This product is hydrolyzed and decarboxylated to 3-(3-methoxybenzoyl)adipic acid by refluxing in aqueous acetic acid containing sulfuric acid by the procedure of Method A of Example XLVII. Corresponding esters are prepared in the usual manner.

EXAMPLE XLVII Diethyl 3-(3-methoxybenzoyl)adipate Method A.A mixture of 25 g. of diethyl-3-carbethoxy-3-(3-methoxybenzoyl)adipate in 30 ml. of acetic acid, 10 ml. of concentrated sulfuric acid and 10 ml. of water is refluxed for 36 hours. The mixture is then poured into excess water and extracted with chloroform, the extract dried and evaporated under reduced pressure to an oil. The oil is dissolved in a mixture of 50 ml. of ethanol, 1 liter of ethylene dichloride and 6 ml. of concentrated sulfuric acid and refluxed for 12 hours. The mixture is then poured into water. The ethylene chloride layer is separated, dried and evaporated in vacuo to an oil which 39 is distilled to obtain 5.5 g. of product, B.P. 169-172 C. (0.05 mm.), n =l.5092.

Elemental analysis gives the following results:

Calcd. for C H O (percent): C, 64.27; H, 7.19. Found (percent): C, 64.09; H, 7.19.

In similar fashion, the dimethyl and dipropyl esters are prepared.

Method B.The product of Example XLV a yellow viscous oil, is refluxed in 120 ml. of dry xylene containing 3.0 g. of p-toluenesulfonic acid and cooled and extracted with water. The xylene solution, after drying, is concentrated under reduced pressure and the residual oil vacuum distilled to obtain 6.8 g. of product.

There is also obtained 5.86 g. of the enol lactone:

ACE;

a red oil, which on infrared absorption analysis showed a maximum at 5.58;.

As is recognized by those in the art, the product of this example is a racemic compound, DL-3-(3-methoxybenzoyl)adipic acid diethyl ester which, as the free acid, lends itself to resolution into its optical active forms by salt formation with optically active bases such as brucine, o

EXAMPLE xLvnI Employing the procedure of Example XL the following compounds are prepared from corresponding starting compounds. Those compounds having an active hydrogen require the use of an additional mole of sodium hydride.

methylbenzoylacetate ethyl (Z-ethyl-S-hydroxybenzoyl)acetate methyl 2-(S-methoxybenzoyl)propionate methyl Z-(S-methoxybenzoyl)butanoate methyl 2-(S-methoxybenzoyl)pentanoate methyl (2-chloro-5-methoxybenzoyl)acetate methyl (Z-dimethylamino--methoxybenzoyl) acetate methyl (Z-amino-S-methoxybenzoyl)acetate methyl (2-acetarnido-S-methoxybenzoyl)acetate ethyl S-hydroxyhenzoyl) acetate ethyl (Z-methoxybenzoyl)acetate ethyl 3-hydroxybenzoyl acetate ethyl (Z-methyl-S-hydroxybenzoyl)acetate ethyl (2,3-dimethyl-S-hydroxybenzoyl)acetate ethyl (3-isopropyl-5-hydroxybenzoyl)acetate ethyl 2,3-diethyl-S-hydroxybenzoyl) acetate ethyl (S-benzyloxybenzoyl)acetate ethyl (3-methyl-5-hydroxybenzoyl)acetate ethyl (3-dimethylamino-S-hydroxybenzoyl)acetate methyl (2,3-dimethylbenzoyl)acetate ethyl (3,5-dimethoxybenzoyl) acetate ethyl (2,3-diethyl-5-ethoxybenzoyl) acetate ethyl (3-isopropyl-5-ethoxybenzoyl)acetate methyl (Z-methylamino-S-methoxybenzoyl)acetate methyl (3-ethyl-5-methoxybenzoyl)acetate ethyl (2-methoxy-S-benzyloxybenzoyl)acetate ethyl (2-propyl-S-propoxybenzoyl)acetate ethyl (3-trifluoromethyl-5-methoxybenzoyl)acetate EXAMPLE XLIX The following carbalkoxybenzoyl propionates are prepared from corresponding benzoyl acetates by reaction with a-haloacetic acid esters according to the procedure of Method A of Example XLII, as well as by the procedure of Method B, Example XLII.

ethyl 3-carbomethoxy-3-benzoylpropionate methyl 3-carbethoxy-3-(2-ethyl-5-methoxybenzoyl) propionate methyl 3-carbomethoxy-3-(3-methoxybenzoyl)butanoate 1 methyl 3-carbomethoxy-3-(3-methoxybenzoyl) pentanoate 1 methyl 3-carbornethoxy-3-(3-rnethoxyhenzoyl) hexanoate 1 methyl 3-carbomethoxy-3-(2-chloro-S-methoxybenzoyl) propionate methyl 3-carbomethoxy-3-(2-dimethylamino-5-methoxybenzoyl)propionate benzyl 3-carbomethoxy-3-(Z-acetamido-S-methoxyhenzoyl)propionate ethyl 3-carbethoxy-3-(S-methoxybenzoyl)propionate ethyl 3-carbethoxy-3-(2,3-diethyl-5-rnethoxyhenzoyl) propionate ethyl 3-carbethoxy-3-(3-isopropyl-5-methoxybenzoyl) propionate ethyl 3-carbethoxy-3-(2-methyl-5-ethoxybenzoyl)propionate ethyl 3-carbethoxy-3-(3-dimethylamino-5-propoxybenzoyl)propionate methyl 3-carbornethoxy-3- 2,3-dimethylbenzoyl propionate ethyl 3-carhethoxy-3-(3-methoxybenzoyl)propionate ethyl 3-carbethoxy-3-(Z-methyl-S-methoxybenzoyl)propionate ethyl 3-carbethoxy-3-(4-methyl5-methoxybenzoyl)pro pionate ethyl 3-carbethoxy-3-(2,3-dimethyl-5-methoxybenzoyl) propionate ethyl 3-carbethoxy-3-(3-benzyloxybenzoyl)propionate ethyl 3-carbethoxy-3- 3 ,5 -dimethoxybenzoyl propionate ethyl 3-carbethoxy-3-(2,3-diethyl-5-ethoxybenzoyl)propionate ethyl 3-carbethoxy-3-(3-isopropyl-5-ethoxybenzoyl)propionate methyl 3-carbomethoxy-3-(Z-methylamino-S-methoxybenzoyl)propionate The higher benzoyl alkanoates, cg. butanoatc, pontanoate and hexanoate, are prepared from the next lower homolog by the procedure of Method A, Example XLII. 

